Next Article in Journal / Special Issue
Evaluation of the Soothing and Protective Properties of a Lignin Hydrolyzate
Previous Article in Journal
Unique Hair Properties that Emerge from Combinations of Multiple Races
Previous Article in Special Issue
Analysis of Heavy Metal Content in Conventional and Herbal Toothpastes Available at Maltese Pharmacies
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Halal Cosmetics: A Review on Ingredients, Production, and Testing Methods

1
Laboratory of Pharmaceutics and Cosmeceutics, School of Pharmacy and Pharmaceutical Sciences, Josai University, Saitama 350-0295, Japan
2
International Center for Halal Studies, Management and Science University, Selangor 40100, Malaysia
3
Department of Pharmacy, Faculty of Health Science, Syarif Hidayatullah State Islamic University Jakarta, Banten 15419, Indonesia
4
School of Pharmacy, Walailak University, Nakhon Si Thammarat 80161, Thailand
5
Department of Pharmacy, University of San Carlos, Cebu 6000, The Philippines
*
Author to whom correspondence should be addressed.
Submission received: 6 June 2019 / Revised: 26 June 2019 / Accepted: 28 June 2019 / Published: 1 July 2019
(This article belongs to the Special Issue Cosmetics: Feature Papers)

Abstract

:
The demand for halal cosmetic products among the 2.4 billion Muslim consumers worldwide is increasing. However, the demand for halal cosmetics remains unmet because cosmetics production is dominated by non-halal cosmetic manufacturers, whose production methods may not conform with the requirements of halal science. The development of halal cosmetics and the assessment of their product performance is still in its infancy. The integration of halal science in the manufacture of most cosmetic products remains inadequate. Moreover, there is a global dearth of guiding documents on the development and assessment techniques in the production of comprehensively halal cosmetics. This paper aims to abridge existing literature and knowledge of halal and cosmetic science in order to provide essential technical guidance in the manufacture of halal cosmetics. In addition, the adoption of these methods addresses the unique ethical issues associated with conformance of cosmetics’ product performance to religious practices and halal science. It highlights the applicability of established methods in skin science in the assessment of halal cosmetics.

1. Introduction

Halal denotes permissible and lawful, whereas haram means prohibited by Islamic law. Najis refers to uncleanliness, analogous to the contamination of something considered halal. Halalan-toyyiban is a concept wherein a product is deemed halal, contains wholesome ingredients, and does not pose any health risk when the product is used. The halal-haram rule is a part of the entire legal system of Islam. The term halal is often associated with food. However, this term essentially includes a wide area apart from food. Halal is relevant in every aspect of a person’s life, such as source of income, attitude towards a product, and religiosity, among others [1]. Halal law prioritizes the importance of the permissibility of food to be consumed, because food intake directly impacts the development of human wellness and behavior. In parallel, consuming haram products (prohibited) is purported to be injurious to one’s physical health and overall character. It is a dictum among Muslims to consume only halal products as this is viewed to affect religiosity [1,2].
Halal pharmaceuticals and cosmetic products are gaining awareness and increasing demand among the 2.4 billion Muslim consumers worldwide. The global halal market is anticipated to expand at a compound annual growth rate of 6.8% until 2024 [3]. Apart from the large Muslim population who exhibit high loyalty to halal products, halal cosmetics carry a wider market appeal among non-Muslim consumers, who attribute these products with ethical consumerism and more stringent quality assurance standards. In addition, for non-Muslims, halal can become a benchmark of accepted conformance and quality in trade dealings with Muslims [1,4].
Halal cosmetic products must not contain ingredients derived from pig, carrion, blood, human body parts, predatory animals, reptiles, and insects among others. Cosmetic ingredients derived from permissible animals must be slaughtered according to Islamic law to be considered halal [4]. In the preparation, processing, manufacture, storage, and transport of halal cosmetic products, maintenance of hygiene and pure conditions must be ensured at all times. There is an emphasis on the absence of filth. The intent of certifying products as halal is parallel with the goals of most quality assurance procedures (e.g., cGMP, HACCP) [1]. Hence, halal cosmetic products, bearing the halal logo, must be recognized as an indicator of cleanliness, safety, purity, and quality.
Although pharmaceutical products have gained scientific advancement way beyond cosmetic products as evidenced by the numerous halal-certified drug products in the market, scientific efforts in the development of cosmetics as a halal product must be probed further to adequately fulfill global demand. For Muslim consumers, knowing the origin of raw materials and the production process of cosmetic ingredients is vital, due to the Islamic law stating that every Muslim must consume only halal and wholesome products [5]. Moreover, scrutinizing cosmetic products can be very challenging and demands technical knowledge of the ingredients, their sources, and manufacturing methods. Cosmetic products are complex and constitute several highly processed products that are manufactured using ingredients of animal or plant origins. Upon application, cosmetic products may be unintentionally ingested (e.g., lipstick), inhaled (e.g., perfumes), or absorbed through the skin (e.g., alcohol or ingredients of critical origin) [6]. With the known challenges, manufacturers have to guarantee that cosmetic products are critically developed to be halal in composition and support holistically the requirements of Islamic rituals (e.g., wudu, cleansing before praying, or reading the Qur’an) performed on a daily basis.
There are several challenges that need to be taken into account in the development of halal cosmetics. Cosmetic ingredients derived from animals such as gelatin, lecithin, glycerol, fatty acids, and collagen are very difficult to verify as halal. Some coloring agents may be derived from insects, hence qualified as haram. Moreover, ingredients that are of bovine origin poses another challenge as the animals may be slaughtered in non-halal manner. Not only the use of halal ingredients is required in the production but also the overall cosmetic product performance, in order to meet requirements of Islamic rituals. A case in point, a lacquered nail must be penetrable by water to allow sufficient rinsing, and cosmetic products applied on skin must also be penetrable to water or be completely rinsed off to allow Muslims to perform their rituals accordingly.
While the detection methods for haram materials are in place, the development of halal cosmetics and the assessment of product performance are still in their infancy. Cosmetics production is dominated by non-halal cosmetic manufacturers [6] whose production methods do not conform to the requirements of halal science, hence, emphasizing the need to develop guiding documents for such purpose. Moreover, there is a global dearth of guiding documents in the development and assessment techniques in the production of comprehensively halal cosmetics. This paper aims to abridge existing literature and knowledge of halal and cosmetic science in order to provide essential technical guidance in the manufacture of halal cosmetics. It highlights the applicability of established methods in skin science in the assessment of halal cosmetics.

2. Source of Halal Cosmetic Ingredients

Halal cosmetics are products, sourced from halal ingredients and produced in accordance with the halal system, intended to be applied on a specific part(s) of the body, whether as leave-on or rinse-off, for the purpose of beautifying, cleansing, protecting, and changing the appearance of the body.
Cosmetics constitute a myriad of ingredients including water, oils, surfactants, polymers, organic solvents, colorants, proteins, vitamins, plant extracts, preservatives, and antioxidants, among others [7]. With the complex mixture of ingredients in a cosmetic product, cosmetic manufacturers must critically evaluate the ingredients and their corresponding source prior to development and production.
The source of ingredients intended for the development and manufacture of halal cosmetics plays a crucial role in the outcome and overall performance of the product. It is the responsibility of manufacturers rather than regulators to substantiate the safety of the ingredients used for halal cosmetic products [8]. Manufacturers have to work closely with suppliers to ensure only halal certified ingredients are being supplied. It should begin with an end in mind that raw materials, actives, or excipients must be obtained from certified sources considered halal. Not only do the ingredients have to be halal, but also safe for consumers for the intended use. This section focuses on the common ingredients used in the preparation of cosmetic products. These ingredients are classified into halal, haram, and critical.

2.1. Halal (Permitted) Cosmetic Ingredients

Halal cosmetic ingredients are any constituents derived from plants, soil, water, permissible animals slaughtered according to Islamic law, marine animals deemed halal, and synthetic materials that are safe for consumers and unadulterated with filth (najis). Table 1 provides a representative list of ingredients considered halal. Plant-derived components and chemical synthesis (precursor compounds) of ingredients are replacing animal-derived ones in the manufacture of halal cosmetics as a means to diminish doubt and to better gain acceptance among consumers. Reducing the number of critical ingredients used in the development of cosmetics facilitates the certification process, because it rules out the incorporation of unacceptable or haram ingredients. As a rule of thumb, manufacturers must secure halal certification for each ingredient from suppliers.
The cosmetic ingredients listed below are classified as halal on the basis that they remain uncontaminated or unadulterated with najis after obtaining and producing them from their halal sources.

2.2. Haram (Prohibited) Cosmetic Ingredients

Haram cosmetic ingredients are any constituents derived from human body parts, blood, forbidden animal parts and insects, and prohibited or restricted chemicals that are harmful or injurious to consumers. Ingredients recognized to be prohibited or restricted by governing bodies in cosmetic products are recognized as haram. Table 2 provides a representative list of ingredients considered haram.

2.3. Critical Cosmetic Ingredients

Cosmetic ingredients are classified under this category if they originate from sources (e.g., unspecified animals, halal animals slaughtered in an unspecified manner) and process of synthesis (e.g., incorporation of haram processing aids, contamination with haram or najis) nonconforming to the halal system. However, the use of alternatively sourced ingredients classified as “critical” may still be allowed to be part of a halal cosmetic product after the manufacturer has secured halal certification for its origin and production, at the same time, uncontaminated with najis. Particularly, the presence of ethanol in cosmetic products is controversial, but according to the Department of Islamic Development Malaysia (JAKIM) and the Assessment Institute for Foods, Drugs and Cosmetics Indonesian Council of Ulama (LPPOM-MUI) [51], cosmetic products may contain ethanol as long as it is sourced from natural aerobic fermentation (i.e., natural fermentation process in the presence of oxygen) or synthetic sources (i.e., prepared from ethylene oxide, acetaldehyde, acetylene) and not from the khamr (liquor) industry. Table 3 provides a representative list of ingredients classified as critical.

2.4. General Guidelines for Halal and Non-Halal Cosmetic Ingredients

Several guiding documents on the requirements for the certification of halal cosmetics exist, and manufacturers must adhere to the set standards alongside with those mentioned in the previous sections of this paper. These documents provide general guidelines in the production and manufacture of cosmetics but incomprehensive on sourcing of ingredients for the manufacture of halal cosmetics, although none about testing of its product performance (i.e., in support of Muslim rituals). The applicability of the guidelines listed in Table 4 may vary depending on the country of production and the target market, manufacturers have to ensure that these are met.

3. Production of Halal Cosmetics

The production of halal cosmetics does not only entail critically sourcing ingredients to be considered halal. The same principle follows through the production of the cosmetic products. Aside from cosmetic manufacturing requirements (e.g., cGMP, ISO among others) that manufacturers have to adhere to, a halal assurance system has to be in place as well.
A form of halal assurance system must be developed and adapted as a requirement in seeking halal certification of the cosmetic product. Its main objective is to sustain the halal production processes to assure compliance to the mandates of halal regulating bodies (e.g., LPPOM-MUI, JAKIM). This assurance system must be applied in all processes in the production of cosmetics, wherein proper documentation of the processes is required. This allows the traceability of each process in the production system. Manufacturers must create an in-house manual for the halal assurance system covering components on the halal policy, halal guidelines, halal management organization, standard operating procedures, technical references, administration system, documentation system, stakeholder engagement, training programs, audit system, corrective action system, and management review system [87].
In this section, we provide points for manufacturers to consider and to ensure that a halal assurance system is in place in the manufacture of halal cosmetics. Accuracy in documentation of these lines of evidence is expected among halal cosmetic manufacturers. Table 5 presents points for consideration in developing a halal assurance system.

Manufacturing, Storing, Packaging, and Distribution

The formulation development of halal cosmetics must begin with ingredients that are undoubtedly of halal origin. Use of alternatively sourced “critical” ingredients (e.g., ethanol, fish-derived collagen, chicken-derived gelatin) must be recognized only when appropriate documents of halal certification are presented. Other critical ingredients of unverified halal certification status are not recommended for use in the manufacture of halal cosmetics.
The manufacture of halal cosmetic products must be produced in accordance with cGMP and other quality standards to assure product quality and safety. The creation of a group of personnel dedicated to the handling and production of halal cosmetics is recommended. The premises must be designed and located in an area with no risk of contamination by non-halal materials (e.g., proper processes and personnel flow, distant from pig farms) [93]. All production facilities are restricted to the manufacture of halal cosmetics products only. It is imperative that processing of non-halal cosmetics must not be done in the same plant to avoid mandatory ritual cleansing (sertu), which may affect operations [93]. Equipment must be dedicated for use only for halal cosmetic production. Contaminated water (e.g., water recycled from sewage treatment, water contaminated with najis) must not be used in the manufacture of halal cosmetics. The composition of cleaning materials (e.g., scrubs, brushes) used in the maintenance of equipment and facilities must not originate from non-halal animals [93]. Manufacturers have to assure that the warehouse and production lines for halal certified and non-halal ones must be physically separated or located in different plants should the manufacturer opt to produce non-halal certified cosmetics. All the processes involved must be clearly labelled with a sign carrying the word halal to prevent them from mix-ups and contamination by non-halal or najis. In addition, care should also be observed to avoid unexpected contamination from the environment (e.g., haram pets) and manpower particulate contamination (e.g., non-halal food or dust).
Halal cosmetic products must be labelled according to the prescribed labelling requirement of the regulatory bodies of each country. The label must bear a halal logo and accurately reflect the ingredients of the product as a means to aid consumer in their decision and consumption of the cosmetic product. Any text, illustrations as well as its advertisement must comply with Islamic law and local culture. The label should not depict lascivious or provocative images as this will automatically qualify the product as haram. The shape of the final product or its package must not exhibit the human body or body parts that are sexually suggestive. A similar tone is recommended in branding of the product. The brand name of halal cosmetics shall not be named or synonymously named after non-halal materials to avoid confusion.
Packaging materials are one of the concerns in the manufacture of halal cosmetics. Materials used in the production of the primary and secondary packaging must also comply with halal standards. Generally, packaging materials are made from halal sources but awareness on the origin of animal-derived ingredients used as aids in the manufacture of packaging must be recognized. Manufacturers of halal cosmetics must secure packaging materials from reputable producers of halal packaging [94]. Product accessories (e.g., application tools, brushes) must not be derived from porcine, human, or other haram materials.
The distribution system has to ensure that halal cosmetic products reach the market maintaining their halal status without being contaminated by haram materials or najis. Halal cosmetic products are recommended to be handled and shipped separately from non-halal ones to avoid cross-contamination.

4. Testing Methods for Halal Cosmetics

In the analysis of halal cosmetics, sourcing of skin model is a major limitation that is unique to the regulations for cosmetics testing, ideals of skin science, and halal systems. Although human or porcine ears are ascribed [95,96,97,98] to be used in the testing of cosmetics, this directly opposes one of the basic tenets of halal science, the absence of human- or porcine-based articles. Consistent with this, the use of rat skin, a competent skin model, or the sacrifice of animals are unacceptable in cosmetics testing as well [99,100,101]. Skin that is of biological origin would have been ideal in this interest owing to its natural barrier function. These limitations overarch into the possible usefulness of artificial model membranes and reconstructed human skin equivalents primarily due to their questionable barrier function [99,102]. Despite these known limitations, a progressive recommendation must be met to allow evaluation of cosmetics suited to be halal. In this paper, we propose the use of silicone model membrane or Strat-M for permeation experiments, which supports the principles of the halal–haram system, data reproducibility, and ease of use. Unavoidably, a 3D reconstructed skin model may be used in determining the distribution of chemicals into stratum corneum (SC) and viable epidermis and dermis (VED).
The methods described for the evaluation of water penetration, skin permeation of alcohol and cosmetic actives of critical origin, and cosmetics “washability” are not yet required by any halal governing bodies, as of the time or writing. However, these methods are viewed to supplement, if not, enhance the assessment of cosmetic products compliant with halal science. Official tests and procedures for the quantification of most cosmetic ingredients have been stipulated in several documents [103,104,105]. The methods described in this paper are intended for the analysis of compounds in the tests discussed herein. This section presents proposed methods for the analysis of halal cosmetic product performance on critical aspects undefined previously.

4.1. Water Penetration through Applied Nail Polish or Hard-to-Wash Cosmetics

Special criteria for halal cosmetics applied to the skin are their ability to allow water penetration. The concept of classifying nail polish as a halal cosmetic product is still a debate. However, there is a clear method that demonstrates the penetrability of specifically designed nail polish with water. “Rinsing” of the nail may be achieved when a substantial amount of water penetrates the applied layer of nail polish and reaches the nail bed. Breathability (air/oxygen) and water vapor permeability have been claimed for water-based nail polish formulations using tests prescribed in DIN 53380-3 and DIN 53122-1 [106]. These tests, however, do not appear to be reflective of actual in-use conditions such as application onto the nail or rinsing prior to rituals.
Assessment of water penetration of nail polish in its applied form may be done in two ways as a combination of previously described works [107,108,109,110]. First, a practical procedure utilizing a Franz diffusion cell and silicone membrane previously applied with nail polish may be employed. A second method being more realistic, suggests the use of human nail, or in this context the use of equivalent material, applied with nail polish and set on a specially designed Franz-type diffusion cell. The temperature of the membrane and nail must be maintained at 32 °C. A finite dose of deuterium oxide (D2O) is applied on the donor side, with the withdrawal of aliquots at predetermined times. Detection of D2O using Fourier-transform infrared spectroscopy should directly confirm water penetration through the applied nail polish.
The same method is viewed to be beneficial in the assessment of water penetration in difficult to wash cosmetics (e.g., lipstick, eye mascara, eye liner). A silicone membrane set on a Franz-type diffusion cell applied with finite dose of D2O should confirm water penetration as well.
This method opens windows of opportunities for current manufacturers of halal ingredient-based nail polish and difficult-to-wash-off cosmetics to revise and improve formulations, and ultimately, gain compliance.

4.2. Determining Permeation of Alcohol, and Solvent/Cosmetic Actives of Critical Origin

The use of ingredients in the development of cosmetic formulation are employed in accordance with its intended purpose. Cosmetic active ingredients are employed mainly for their purported activity (e.g., skin whitening, anti-aging). Excipients (e.g., ethanol, other solvents) are incorporated to promote solubility of the actives/partitioning into the SC or simply for enhanced tactile impression or psychorheology. It must be noted that ethanol is allowed in topical formulations for use among Muslims provided it does not exceed 1% [80]. Absorption into the skin of solvents with doubtful origin such as ethanol and glycerin are well documented [81,111,112,113].
Functional cosmetics (contains quasi-drug actives) are now common in the market and have become the preferred way of delivering actives with purported skin enhancement effects. In fact, they are sold in sets (i.e., cleanser, lotion, milk, essence) and are recommended to be applied in layers in a predefined sequence.
Detection and quantification of cosmetic actives in skin (SC and VED) following dermal absorption has long been established [96,97,98,99,100,108,114,115]. Quantification of cosmetic actives permeating through the skin following actual in-use conditions, such as layered application, has been reported recently [116]. Together, these methods could provide insights into product formulation development with respect to the permeation of ingredients. Manipulating the proportions of ingredients in the formulation or the use of retardants could reveal an ideal formulation that could significantly reduce or eliminate absorption through skin of alcohol, solvent/cosmetic actives of critical origin (e.g., collagen, gelatin, glycerin). Analytical methods described in this section could ascertain whether critical ingredients are absorbed or not. In addition, the evaporation of alcohol and other solvents can be evaluated to clarify its behavior (i.e., permeation or evaporation) once applied on skin [111,112,117].
In the determination of ethanol permeation, radiolabeled ethanol (14C-ethanol) is suggested to be used in the formulation in place of regular ethanol. Permeation experiments for ethanol and other ingredients of concern may be carried out in Franz-type diffusion cells as reported previously [107,112]. In addition, gravimetric techniques have been reported in estimating evaporation of neat ethanol from formulations [112,118].
Realistic evaluation of chemical permeation can be attained when conditions closely simulating actual use conditions are employed [119]. The use of a finite dose and the manner of formulation application (in membrane) must be reflective of actual in-use conditions (e.g., layered application, defined sequence). Sampling from the receiver chamber is then performed as described above. The instrumental detection and quantification of compounds investigated may be performed as described previously. For reference, we summarized instrumental quantification conditions in skin permeation experiments for some cosmetic ingredients classified as critical (Table 6).

4.3. Cosmetics “Washability” Quantification

The ability of applied cosmetics to be washed off is of paramount significance with physical purity. This principle is of great value in the observance of wudu and encouraged prior to the reading of the Qur’an. In fact, many cosmetics (e.g., body lotion, face cream, nail polish, eye mascara among others) are applied as “leave on” cosmetics and adhere on the skin for a long time [123]. “Washability” of applied cosmetics can be realistically simulated using a simple procedure described in a previous work [124]. Concisely, applied cosmetics on the skin is rinsed first with water, and wiped off with a cotton swab previously dampened with sodium lauryl sulfate (0.5%) to mimic consumer use of liquid soap. Lastly, the skin may be rinsed with water to reflect terminal rinsing during bathing or washing.
To ultimately validate the washability of applied cosmetics, dermatopharmacokinetics and tissue distribution studies could validate the deposition of chemicals in the SC and VED, if any, may be done. A previous work presented a practical method for the quantification of chemicals deposited on the SC and hair follicles after topical application [125]. It suggests stripping of the SC 20 times using cellophane tape, extraction of drug from the tape with ethanol, and vortexing for 1 h. Tissue distribution is established by cutting and homogenizing the resulting VED. Quantification may proceed as described elsewhere [125].

5. Detection of Haram Ingredients in Cosmetics

Halal-based “purity” of materials and products is the basis for authenticity of halal products. In this study, we have identified new, yet relevant, methods for qualifying cosmetic products claiming to be halal-compliant.
Compliance should not be viewed only as an oversimplification of the absence or presence of something haram in a product. Rather, one must not neglect the actual product performance and how it interacts with a Muslim’s daily rituals. In this manner, products are developed to be halal with an assurance both in composition and performance.
This section presents numerous works made in contribution to promote halal science, halal product quality, and compliance, and efforts in safeguarding the religious interests of Muslims. Methods of detecting haram ingredients, predominantly the presence of porcine-based materials, have been extensively studied [2]. Detection techniques are broadly categorized as chromatographic; high-performance liquid chromatography (HPLC) [126,127], reversed-phase HPLC [128], HPLC–tandem mass spectrometry (MS) [129], ultra-performance liquid chromatography-time-of-flight MS [130], ultra-performance liquid chromatography-electrospray ionization quadrupole time-of-flight MS [131], HPLC/MS linear ion trap/Orbitrap [132], liquid chromatography–tandem MS (LC–MS/MS) [133], and Fourier-transformed infrared spectroscopy [134], or biochemical techniques; conventional duplex polymerase chain reaction (PCR) [135], multiplex PCR-restriction fragment length polymorphism [136], sodium dodecyl sulfate-polyacrylamide gel electrophoresis [137], and calcium phosphate precipitation [138]. A recently developed method using LC–MS/MS claims to significantly reduce sample preparation time and presents excellent sensitivity to a high number of specific peptide markers differentiating materials of bovine and porcine origin [133]. Moreover, the use of a high-performance gas chromatography–time of flight MS with a lipid library search feature allows discrimination of the origin of ingredients. In addition, it has been reported to have isotope pattern analysis resulting in high sensitivity and high mass accuracy of the analytes [4].
It is not the intention of this paper to prescribe analytical techniques for the detection of haram materials but it encourages the use of the described methods, as is feasible with the institution’s analytical capacity. Ultimately, any raw materials or finish products can be tested using the tests described above to rule out the presence of haram materials.

6. Conclusions

The development of halal cosmetics encompasses the concept of critically sourcing halal ingredients, applying halal practices in every step of the manufacturing process, and ensuring conformance of product performance to Islamic rituals. This document sheds light on the methods to assess previously disputed concepts in cosmetics and strengthens the existing testing methods in the assessment of halal cosmetics. The use of scientific methods in the development of halal cosmetics must be advanced to ascertain the halal status and promote market acceptance not only among Muslim consumers but also by non-Muslims as well. Halal cosmetics transcends beyond religion because they require rigorous scientific investigation to come up with a product that is safe, effective, pure, and sensitive to the holistic needs of the Muslim community.

Author Contributions

Conceptualization, K.S., G.L.S., F.J.A. and S.D.; methodology, K.S., H.T., G.L.S., F.J.A., S.D.; resources, E.Y., K.S., H.T., P.S.; writing—Original draft preparation, all authors; writing—review and editing, all authors; visualization, all authors; supervision, K.S., H.T., E.Y.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Hashim, P.; Mat Hashim, D. A review of cosmetic and personal care products: Halal perspective and detection of ingredient. Pertanika J. Sci. Technol. 2013, 21, 281–292. [Google Scholar]
  2. Hassan, N.; Ahmad, T.; Zain, N.M. Chemical and chemometric methods for halal authentication of gelatin: an overview. J. Food Sci. 2018, 83, 2903–2911. [Google Scholar] [CrossRef] [PubMed]
  3. Trent, N. Halal Cosmetics Market 2018-Industry Analysis, Share, Growth, Sales, Trends, Supply, Forecast to 2025. Reuters. Available online: https://www.reuters.com/brandfeatures/venture-capital/article?id=52417 (accessed on 10 March 2019).
  4. Yusuf, E.; Yajid, M.S.A. Related topic: Halal Cosmetics. In Skin Permeation and Disposition of Therapeutic and Cosmeceutical Compounds; Sugibayashi, K., Ed.; Springer: Tokyo, Japan, 2017; pp. 101–107. [Google Scholar]
  5. Briliana, V.; Mursito, N. Exploring antecedents and consequences of Indonesian Muslim youths’ attitude towards halal cosmetic products: A case study in Jakarta. Asia Pac. Manag. Rev. 2017, 22, 176–184. [Google Scholar] [CrossRef]
  6. Houlis, A. Halal Cosmetics: Control of Ingredients. Available online: https://www.sigmaaldrich.com/technical-documents/articles/white-papers/flavors-and-fragrances/halal-ingredients-sources-cosmetics.html (accessed on 2 February 2019).
  7. Iwata, H.; Shimada, K. Developing the formulations of cosmetics. In Formulas, Ingredients and Production of Cosmetics: Technology of Skin-and Hair-care Products in Japan; Iwata, H., Shimada, K., Eds.; Springer: Tokyo, Japan, 2013; pp. 21–86. [Google Scholar]
  8. Dent, M.; Amaral, R.T.; Silva, P.A.; Ansell, J.; Boisleve, F.; Hatao, M.; Hirose, A.; Kasai, Y.; Kern, P.; Kreiling, R.; et al. Principles underpinning the use of new methodologies in the risk assessment of cosmetic ingredients. Comput. Toxicol. 2018, 7, 20–26. [Google Scholar] [CrossRef]
  9. Li, Y.; Dong, C.; Cun, D.; Liu, J.; Xiang, R.; Fang, L. Lamellar liquid crystal improves the skin retention of 3-O-ethyl-ascorbic acid and potassium 4-methoxysalicylate in vitro and in vivo for topical preparation. AAPS PharmSciTech 2016, 17, 767–777. [Google Scholar] [CrossRef] [PubMed]
  10. Ito, S.; Wakamatsu, K. A convenient screening method to differentiate phenolic skin whitening tyrosinase inhibitors from leukoderma-inducing phenols. J. Dermatol. Sci. 2015, 80, 18–24. [Google Scholar] [CrossRef] [PubMed]
  11. Ivica, C.; Litvić, M. Simple and efficient synthesis of arbutin. Arkivoc 2008, 2, 19–24. [Google Scholar]
  12. Maeda, K.; Fukuda, M. Arbutin: Mechanism of its depigmenting action in human melanocyte culture. J. Pharmacol. Exp. Ther. 1996, 276, 765–769. [Google Scholar]
  13. Kumar, N.; Pruthi, V. Potential applications of ferulic acid from natural sources. Biotechnol. Rep. (Amst.) 2014, 4, 86–93. [Google Scholar] [CrossRef] [Green Version]
  14. Chien, C.W.; Teng, Y.H.G.; Honda, T.; Ojima, I. Synthesis of colchicinoids and allocolchicinoids through Rh(I)-Catalyzed [2+2+2+1] and [2+2+2] Cycloadditions of o-Phenylenetriynes with and without CO. J. Org. Chem. 2018, 83, 11623–11644. [Google Scholar] [CrossRef]
  15. Kadokawa, J.; Nishikura, T.; Muraoka, R.; Tagaya, H.; Fukuoka, N. Synthesis of Kojic Acid Derivatives Containing Phenolic Hydroxy Groups. Synth. Commun. Int. J. Rapid Commun. Synth. Org. Chem. 2003, 33, 1081–1086. [Google Scholar]
  16. Liu, X.; Xia, W.; Jiang, Q.; Xu, Y.; Yu, P. Synthesis, characterization, and antimicrobial activity of kojic acid grafted chitosan oligosaccharide. J. Agric. Food Chem. 2014, 62, 297–303. [Google Scholar] [CrossRef] [PubMed]
  17. Guiso, M.; Marra, C.; Farina, A. A new efficient resveratrol synthesis. Tetrahedron Lett. 2002, 43, 597–598. [Google Scholar] [CrossRef]
  18. Li, Z.; Fang, L.; Dong, L.; Guo, Y.; Xie, Y. An improved and practical synthesis of tranexamic acid. Org. Process. Res. Dev. 2015, 19, 444–448. [Google Scholar] [CrossRef]
  19. Everts, S. Green chemistry environmentally friendly synthesis of niacin generates less inorganic waste. Chem. Eng. News 2008, 86, 15. [Google Scholar] [CrossRef]
  20. Linster, C.L.; Van Schaftingen, E.; Vitamin, C. Biosynthesis, recycling and degradation in mammals. FEBS J. 2007, 274, 1–22. [Google Scholar] [CrossRef]
  21. Yamano, Y.; Ito, M. Total synthesis of capsanthin and capsorubin using Lewsi acid-promoting regio-and stereoselective rearrangement of tetrasubstituted epoxides. Org. Biomol. Chem. 2007, 5, 3207–3212. [Google Scholar] [CrossRef]
  22. Goszcz, K.; Deakin, S.J.; Duthie, G.G.; Stewart, D.; Megson, I.L. Bioavailable concentrations of delphindin and its metabolite, gallic acid, induce antioxidant protection associated with increased intracellular glutathione in cultured endothelial cells. Oxid. Med. Cell Longev. 2017, 2017, 9260701. [Google Scholar] [CrossRef]
  23. Aouf, C.; Nouailhas, H.; Fache, M.; Caillol, S.; Boutevin, B.; Fulcrand, H. Multi-functionalization of gallic acid. Synthesis of a novel bio-based epoxy resin. Eur. Polym. J. 2013, 49, 1185–1195. [Google Scholar] [CrossRef]
  24. Xiong, P.; Wang, R.; Zhang, X.; Dela Torre, E.; Leon, F.; Zhang, Q.; Zheng, S.; Wang, G.; Chen, Q.H. Design, synthesis, and evaluation of genistein analogues as anti-cancer agents. Anticancer. Agents Med. Chem. 2015, 15, 1197–1203. [Google Scholar] [CrossRef]
  25. Brieskorn, C.H.; Sax, H. Synthesis of glycyrrhizin and glycyrrhetin acid derivatives. Pharm. Ges. 1970, 303, 905–912. [Google Scholar]
  26. Kim, J.; Della Penna, D. Defining primary route for lutein synthesis in plants: The role of Arabidopsis carotenoid B-ring hydroxylase CYP97A3. Proc. Natl. Acad. Sci. USA 2006, 103, 3474–3479. [Google Scholar] [CrossRef] [PubMed]
  27. Wang, L.; Li, Z.W.; Zhang, W.; Xu, R.; Gao, F.; Liu, Y.F.; Li, Y.J. Synthesis, crystal structure, and biological evaluation of a series of phloretin derivatives. Molecules 2014, 19, 16447–16457. [Google Scholar] [CrossRef] [PubMed]
  28. Guo, Y.; Zhao, Y.; Zheng, C.; Meng, Y.; Yang, Y. Synthesis, biological activity of salidroside and its analogues. Chem. Pharm. Bull. 2010, 58, 1627–1629. [Google Scholar] [CrossRef]
  29. Schalk, M.; Pastore, L.; Mirata, M.A.; Khim, S.; Schouwey, M.; Dequerry, F.; Pineda, V.; Rocci, L.; Daviet, L. Towards biosynthetic route to sclareol and amber odorants. J. Am. Chem. Soc. 2012, 134, 18900–18903. [Google Scholar] [CrossRef] [PubMed]
  30. Barrero, A.F.; Siméon, A.; del Moral, J.F.Q.; Herrador, M.M.; Valdivia, M.; Jimenez, D. First synthesis of the antifungal oidiolactone C from trans-commumnic acid: Cytotoxic and antimicrobial activity in podolactone-related compounds. J. Org. Chem. 2002, 67, 2501–2508. [Google Scholar] [CrossRef] [PubMed]
  31. Maimba, O. Umbelliferone: Synthesis, chemistry and bioactivities review. Bull. Fac. Pharm. Cairo Univ. 2017, 55, 223–232. [Google Scholar] [CrossRef]
  32. Shui, T.; Feng, S.; Chen, G.; Li, An.; Yuan, Z.; Shui, H.; Kuboki, T.; Xu, C. Synthesis of sodium carboxymethyl cellulose using bleached crude cellulose fractioned from cornstalk. Biomass Bioenergy 2017, 105, 51–58. [Google Scholar] [CrossRef]
  33. Yu, X.; Wang, N.; Zhang, R.; Zhao, Z. Simple synthesis hydrogenated castor oil fatty amide wax and its coating characterization. J. Oleo Sci. 2017, 66, 659–665. [Google Scholar] [CrossRef]
  34. Zia, K.M.; Tabasum, S.; Nasif, M.; Sultan, N.; Aslam, N.; Noreen, A.; Zuber, M. A review on synthesis, properties and applications of natural polymer based carrageenan blends and composites. Int. J. Biol. Macromol. 2017, 96, 282–301. [Google Scholar] [CrossRef]
  35. Battarjee, S.M.; Abd El-Azim, W.M.; Mohamed, A.A. Preparation of medicinal petroleum jelly using local petroleum waxes. Lubr. Sci. 1999, 12, 89–104. [Google Scholar] [CrossRef]
  36. Yusuf, M.; Shabbir, M.; Mohammad, F. Natural colorants: Historical, processing, and sustainable prospects. Nat. Prod. Bioprospect. 2017, 7, 123–145. [Google Scholar] [CrossRef] [PubMed]
  37. Qin, X.; Zhong, J. A review of extraction techniques for avocado oil. J. Oleo Sci. 2016, 65, 881–888. [Google Scholar] [CrossRef] [PubMed]
  38. Costagli, G.; Betti, M. Avocado oil extraction processes: Method for cold-pressed high quality edible oil production versus traditional production. J. Agric. Eng. 2015, 46, 115–122. [Google Scholar] [CrossRef]
  39. Ni, S.; Zhao, W.; Zhang, Y.; Gasmalla, M.A.A.; Yang, R. Efficient and eco-friendly extraction of corngerm oil using aqueous ethanol solution assisted by steam explosion. J. Food Sci. Technol. 2016, 53, 2018–2116. [Google Scholar] [CrossRef] [PubMed]
  40. Meshram, P.D.; Puri, R.V.; Patil, A.L.; Gite, V.K. Synthesis and characterization of modified cottonseed oil based polyesteramide for coating applications. Prog. Org. Coat. 2013, 76, 1144–1150. [Google Scholar] [CrossRef]
  41. Liu, X.; Zhao, W.; Xiao, F.; Wei, W.; Sun, Y. One-pot synthesis of propylene glycol and dipropylene glycol over strong basic catalyst. Catal. Commun. 2010, 11, 675–678. [Google Scholar] [CrossRef]
  42. Sandha, G.K.; Swami, V.K. Jojoba oil as an organic, shelf stable standard oil-phase base for cosmetic industry. Rasayan J. Chem. 2009, 2, 300–306. [Google Scholar]
  43. Klaus, E.E.; Tewksbury, E.J.; Fenske, M.R. Preparation, properties and some applications of super-refined mineral oils. ASLE Trans. 1962, 5, 115–125. [Google Scholar] [CrossRef]
  44. Morrison, D.S.; Schmidt, J.; Paulli, R. The scope of mineral oil in personal care products and its role in cosmetic formulation. J. Appl. Cosmetol. 1996, 14, 111–118. [Google Scholar]
  45. Li, J.; Kao, W.J. Synthesis of polyethylene glycol (PEG) derivatives and PEGylated–peptide biopolymer conjugates. Biomacromolecules 2003, 4, 1055–1067. [Google Scholar] [CrossRef] [PubMed]
  46. Han, X.; Cheng, L.; Zhang, R.; Bi, J. Extraction of safflower seed oil by supercritical CO2. J. Food Eng. 2000, 92, 370–376. [Google Scholar] [CrossRef]
  47. Corso, M.P.; Fagundes–Klen, M.R.; Silva, E.A.; Filho, L.C.; Santos, J.N.; Freitas, L.S.; Dariva, C. Extraction of sesame seed (Sesamim indicum L.) oil using compressed propane and supercritical carbon dioxide. J. Supercrit Fluid 2010, 52, 56–61. [Google Scholar] [CrossRef]
  48. Prohibited and Restricted Chemicals in Cosmetics. Available online: https://www.fda.gov/Cosmetics/GuidanceRegulation/LawsRegulations/ucm127406.htm (accessed on 1 February 2019).
  49. Hepburn, H.R. Composition and Synthesis of Beeswax. In Honeybees and Wax; Springer: Berlin/Heidelberg, Germany, 1986; pp. 44–56. [Google Scholar]
  50. Kim, T.; Kim, S.; Kang, W.Y.; Baek, H.; Jeon, H.Y.; Kim, B.Y.; Kim, C.G.; Kim, D. Porcine amniotic fluid as possible antiwrinkle cosmetic agent. Korean J. Chem. Eng. 2011, 28, 1839–1843. [Google Scholar] [CrossRef]
  51. Fatwa of Majelis Ulama Indonesia (MUI) No.: 11/2009. 18 November 2009. Available online: http://halalmui.org/images/stories/Fatwa/fatwa-alkohol.pdf (accessed on 10 January 2019).
  52. Cativiela, C.; Fraille, J.M.; Garcia, J.I.; Lázaro, B.; Mayoral, J.A.; Pallarés, A. Heterogeneous catalysis in the synthesis and reactivity of allantoin. Green Chem. 2003, 5, 275–277. [Google Scholar] [CrossRef]
  53. Babilas, P.; Knie, U.; Abels, C. Cosmetic and dermatologic use of alpha hydroxy acids. J. Ger. Soc. Dermatol. 2012, 10, 488–491. [Google Scholar] [CrossRef]
  54. Bhalla, T.C.; Kumar, V.; Bhatia, S.K. Hydroxy acids: Production and applications. In Advances in Industrial Biotechnology; Singh, R.S., Pandey, A., Larroche, C., Eds.; IK International Publishing House PVT. Ltd.: New Delhi, India, 2013; pp. 56–76. [Google Scholar]
  55. Nazzaro-Porro, M. Azelaic acid. In Dermatology in Five Continents; Orfanos, C.E., Stadler, R., Gollnick, H., Eds.; Springer: Berlin/Heidelberg, Germany, 1998; pp. 194–195. [Google Scholar]
  56. Zhang, P.; Tang, Y.; Li, N.G.; Zhu, Y.; Duan, J.A. Bioactivity and chemical synthesis of caffeic acid phenethyl ester and its derivatives. Molecules 2014, 19, 16458–16476. [Google Scholar] [CrossRef]
  57. Lin, Y.; Yan, Y. Biosynthesis of caffeic acid in Escherichia coli using its endogenous hydroxylase complex. Microb. Cell Fact. 2012, 11, 1–9. [Google Scholar] [CrossRef]
  58. Rodríguez, M.I.A.; Barroso, L.G.R.; Sánchez, M.L. Collagen: A review on its sources and potential cosmetic applications. J. Cosmet. Dermatol. 2017, 17, 20–26. [Google Scholar] [CrossRef]
  59. Sze, J.H.; Brownlie, J.C.; Love, C.A. Biotechnological production of hyaluronic acid: A mini review. 3 Biotech 2016, 6, 67. [Google Scholar] [CrossRef]
  60. Mokrejš, P.; Hutta, M.; Pavlačkova, J.; Egner, P. Preparation of keratin hydrosylate from chicken feathers and its application in cosmetics. J. Vis. Exp. 2017, 129, e56254. [Google Scholar]
  61. Rouse, J.G.; Dyke, M.E.V. A review of keratin-based niomaterials for biomedical applications. Materials 2010, 3, 999–1014. [Google Scholar] [CrossRef]
  62. Couteau, C.; Coiffard, L. Overview of skin whitening agents: Drugs and cosmetic products. Cosmetics 2016, 3, 27. [Google Scholar] [CrossRef]
  63. Shcagen, S.K. Topical peptide treatments with effective anti-aging results. Cosmetics 2017, 4, 16. [Google Scholar]
  64. Knott, A.; Achterberg, V.; Smuda, C.; Mielke, H.; Sperling, G.; Dunckelmann, K.; Vogelsang, A.; Krüger, A.; Schwengler, H.; Behtash, M.; et al. Topical treatment with coenzyme Q10-containing formulas improves skin’s Q10 level and provides antioxidative effects. Biofactors 2015, 41, 383–390. [Google Scholar] [CrossRef] [PubMed]
  65. Hojerová, J. Coenzyme Q10–its importance, properties and use in nutrition and cosmetics. Ceska Slov. Farm. 2000, 49, 119–123. [Google Scholar] [PubMed]
  66. Meessen, J. Urea synthesis. Chem. Ing. Tech. 2014, 86, 2180–2189. [Google Scholar] [CrossRef]
  67. Netscher, T. Synthesis of vitamin E. Vitam. Horm. 2007, 76, 155–202. [Google Scholar]
  68. Draget, K.I.; Haug, I.J.; Aasmund, S. Gel-Containing Topical Composition. U.S. Patent Application Publication No. 2009/0131541 A1, 11 May 2009. [Google Scholar]
  69. Alvarez, A.M.R.; Rodríguez, M.L.G. Lipids in pharmaceutical and cosmetic preparations. Grasas Aceites 2000, 51, 74–96. [Google Scholar]
  70. Lopes, B.D.; Lessa, V.L.; Silva, B.M.; La Cerda, L.G. Xanthan gum: Properties, production conditions, quality and economic perspective. J. Food Nutr. Res. 2015, 54, 185–194. [Google Scholar]
  71. Imanaka, H.; Ando, H.; Ryu, A.; Shigeta, Y.; Kishida, S.; Mori, A.; Makino, T. Liposomal linoleic acid is useful as a skin lightening agent. J. Soc. Cosmet. Chem. Jpn. 1999, 33, 277–282. [Google Scholar] [CrossRef]
  72. Nagai, J.; Block, K. Synthesis of oleic acid by Euglena gracilis. J. Biol. Chem. 1965, 240, 3702–3703. [Google Scholar] [PubMed]
  73. Abdul Rahman, M.B.A.; Yap, C.L.; Dzulkefly, K.; Abdul Rahman, R.N.Z.; Salleh, A.B.; Basri, M. Synthesis of palm kernel oil alkanolamide using lipase. J. Oleo Sci. 2003, 52, 65–72. [Google Scholar] [CrossRef]
  74. Zhen, Z.; Xi, T.F.; Zheng, Y.F. Surface modification by natural biopolymer coatings on magnesium alloys for biomedical applications. In Surface Modification of Magnesium and Its Alloys for Biomedical Applications Volume II; Sanarka Narayan, T.S.N., Park, I.S., Lee, M.H., Eds.; Woodhead Publishing: Boca Raton, FL, USA, 2015; pp. 301–333. [Google Scholar]
  75. Popa, O.; Bábeanu, N.E.; Popa, I.; Nita, S.; Dinu-Parvu, C.E. Methods for obtaining and determination of squalene from natural sources. BioMed Res. Int. 2015, 2015, 367202. [Google Scholar] [CrossRef] [PubMed]
  76. Youtz, M. Rapid preparation of cetyl alcohol. J. Am. Chem. Soc. 1925, 47, 2252–2254. [Google Scholar] [CrossRef]
  77. Guo, W.; Sheng, J.; Zhao, H.; Feng, X. Metabolic engineering of Saccharomyces cerevisiae to produce 1-hexadecanol from xylose. Microb. Cell Fact. 2016, 15, 1–11. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  78. Mutlu, V.N.; Yilmaz, S. Esterification of cetyl alcohol with palmitic acid over WO3/Zr-SBA-15 and Zr-SBA-15 catalysts. Appl. Catal. A 2016, 522, 194–200. [Google Scholar] [CrossRef]
  79. Schlossman, M.L.; McCarthy, J.P. Lanolin and its Derivatives. J. Am. Oil Chem. Soc. 1977, 55, 447–450. [Google Scholar] [CrossRef]
  80. Alzeer, J.; Hadeed, K.A. Ethanol and its halal status in food industries. Trends Food Sci. Technol. 2016, 58, 14–20. [Google Scholar] [CrossRef]
  81. DFG, Deutsche Forschungsgemeinschaft. Glycerin. In The MAK–Collection Part. I: MAK Value Documentations; Wiley-VCH GmbH & Co.: KGaA, Weinheim, 2015; Available online: https://onlinelibrary.wiley.com/doi/pdf/10.1002/3527600418.mb5681kske4215 (accessed on 1 January 2019).
  82. Seretis, A.; Tsiakaras, P. Hydrogenolysis of glycerol to propylene glycol by in situ produced hydrogen from aqueous phase reforming of glycerol over SiO2–Al2O3 supported nickel catalyst. Fuel Process. Technol. 2016, 142, 135–146. [Google Scholar] [CrossRef]
  83. Rabello, C.R.K.; Gomes, M.J.; Siqueira, B.G.; De Menezes, R.B.; Huziwara, W.K.; Yamada, T.S.; De Oliveira, L.M.M.; Oliveira, G.C.; Candido, W.V.C. Production of Propylene Glycol from Glycerol. European Patent Application EP 2540692 A2, 2013. Available online: https://patentimages.storage.googleapis.com/df/69/ae/f723554e9b191e/EP2540692A2.pdf (accessed on 2 January 2019).
  84. International Organization for Standardization ISO. Cosmetics–Good Manufacturing Practices (GMP)–Guidelines on Good Manufacturing Practices; ISO 22716; ISO: Geneva, Switzerland, 2007; Available online: https://www.sis.se/api/document/preview/909264/ (accessed on 31 December 2018).
  85. Standard and Metrology Institute for Islamic Countries (SMIIC). Halal Cosmetics–General Requirements; OIC/SMIIC 4:2018; SMIIC: Bakırköy/İstanbul, Turkey, 2018. [Google Scholar]
  86. Gulf Cooperation Council Standardization Organization-Safety Requirements for Cosmetics and Personal Care Products. GSO 12/ DS 1943. 2015. Available online: http://www.puntofocal.gov.ar/notific_otros_miembros/yem3_t.pdf (accessed on 12 January 2019).
  87. General Guidelines of Halal Assurance System. LPPOM MUI, Majelis Ulama, Indonesia. 2012. Available online: https://www.halalcertifiering.se/newwebsiteimages/ebookhashaki.pdf (accessed on 10 December 2018).
  88. ASEAN Guidelines for Cosmetic Good Manufacturing Practice. Available online: https://ww2.fda.gov.ph/attachments/category/197/Appendix%20VI_CosmeticGMP.pdf (accessed on 2 February 2019).
  89. Department of Standards Malaysia, MS2200. Part I: Islamic Consumer Goods–Part 1: Cosmetics and Personal Care–General Guidelines, Standard Malaysia. 2008. Available online: https://law.resource.org/pub/my/ibr/ms.2200.1.e.2008.pdf (accessed on 8 December 2018).
  90. National Pharmaceutical Regulatory Division, Ministry of Health, Malaysia. Drug Registration Guidance Document, 2nd ed.2019. Available online: https://www.npra.gov.my/images/Guidelines_Central/guideline-DRGD/CompleteDRGDwithappendices.pdf (accessed on 2 February 2019).
  91. Guidance for Industry: Cosmetic Good Manufacturing Practices. U.S. Department of Health and Human Services. US FDA. 2013. Available online: https://www.fda.gov/media/86366/download (accessed on 11 January 2019).
  92. Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients. Guidance for Industry. International Council for Harmonization. 2016. Available online: https://www.fda.gov/media/71518/download (accessed on 10 January 2019).
  93. Department of Standards Malaysia, JSM 16/ISC/I-02R1. Halal Cosmetics-General Requirements. 2018. Available online: http://www.jsm.gov.my/documents/10180/2793318/JSM16-MS2200Halal+Cosmetics_21Mar2018.pdf/ca0cca15-c0e7-431e-ab60-debe532c2772 (accessed on 12 February 2019).
  94. Talib, M.S.A.; Johan, M.R.M. Issues in halal packaging: A conceptual paper. Int. Bus. Manag. 2012, 5, 94–98. [Google Scholar]
  95. Jung, E.C.; Maibach, H. Animal models for percutaneous absorption. In Topical Drug Bioavailability, Bioequivalence, and Penetration; Shah., V.P., Ed.; Springer Science + Business Media: New York, NY, USA, 2014; pp. 21–30. [Google Scholar]
  96. OECD. Organization for Economic Cooperation and Development; Guidance 428: Skin Absorption; OECD Press: Paris, France, 2004; p. 8. Available online: https://ntp.niehs.nih.gov/iccvam/suppdocs/feddocs/oecd/oecdtg428-508.pdf (accessed on 9 January 2019).
  97. OECD. Organization for Economic Cooperation and Development; Guidance Document for the Conduct of Skin Absorption Studies # 28; OECD Press: Paris, France, 2004; p. 14. Available online: https://www.oecd-ilibrary.org/docserver/9789264078796-en.pdf?expires=1559264519&id=id&accname=oid006932&checksum=650D34675626065E96BA28CE26628795 (accessed on 19 January 2019).
  98. OECD. Organization for Economic Cooperation and Development; Guidance Notes on Dermal Absorption; Series on Testing and Assessment # 156; OECD Press: Paris, France, 2011; p. 26. Available online: https://www.oecd.org/chemicalsafety/testing/48532204.pdf (accessed on 12 January 2019).
  99. SCCS/1416/11, 2012. The SCCS’s Notes of Guidance for the Testing of Cosmetic Ingredients and Their Safety Evaluation, 9th Revision. Scientific Committee on Consumer Safety. 2016. Available online: http://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_o_190.pdf (accessed on 12 February 2019).
  100. SCCS/1358/10, 2010. Basic Criteria for the in Vitro Assessment of Dermal Absorption of Cosmetic Ingredients. Scientific Committee on Consumer Safety. 2010, p. 8. Available online: https://ec.europa.eu/health/scientific_committees/consumer_safety/docs/sccs_s_002.pdf (accessed on 13 January 2019).
  101. Todo, H. Transdermal permeation of drugs in various animal species. Pharmaceutics 2017, 9, 33. [Google Scholar] [CrossRef] [PubMed]
  102. Flaten, G.E.; Palac, Z.; Engesland, A.; Filipović-Grčić, J.; Vanić, Ž.; Škalko-Basnet, N. In vitro skin models as a tool in optimization of drug formulation. Eur. J. Pharm. Sci. 2015, 75, 10–24. [Google Scholar] [Green Version]
  103. Sixth Commission Directive 95/32/EC Relating to Methods of Analysis Necessary for Checking the Composition of Cosmetic Products. European Union. Official Journal of the European Communities. 1995. Available online: https://publications.europa.eu/en/publication-detail/-/publication/f03d7204-0256-44a5-92be-265a88274047/language-en (accessed on 31 December 2018).
  104. Cosmetics Analytical Methods-Validation Criteria for Analytical Results Using Chromatographic Techniques. ISO 1278. 2011. Available online: https://www.sis.se/api/document/preview/914189/ (accessed on 12 February 2019).
  105. Chisvert, A.; Salvador, A.; Benedé, J.L.; Miralles, P. Tanning and whitening agents in cosmetics: Regulatory aspects and analytical methods. In Analysis of Cosmetic Products, 2nd ed.; Salvador, A., Chisvert, A., Eds.; Elsevier Science: New York, NY, USA, 2017; pp. 107–121. [Google Scholar]
  106. Schlay, S.; Schacht, K.; Storzer, U. Breathable nail polish on the basis of a new blend: A complex of water-based polymer and functional vegan silk. SOFW J. 2017, 143, 56–60. [Google Scholar]
  107. Horita, D.; Todo, H.; Sugibayashi, K. Effect of ethanol pretreatment on skin permeation of drugs. Biol. Pharm. Bull. 2012, 35, 1343–1348. [Google Scholar] [CrossRef] [PubMed]
  108. Sugibayashi, K.; Todo, H.; Oshizaka, T.; Owada, Y. Mathematical model to predict skin concentration of drugs: Toward utilization of silicone membrane to predict skin concentration of drugs as an animal testing alternative. Pharm. Res. 2010, 27, 134–142. [Google Scholar] [CrossRef] [PubMed]
  109. Gunt, H.; Kasting, G. Effect of hydration on the permeation of ketoconazole through human nail plate in vitro. Eur. J. Pharm. Sci. 2007, 32, 254–260. [Google Scholar] [CrossRef]
  110. Okumura, M.; Sugibayashi, K.; Ogawa, K.; Morimoto, Y. Skin permeability of water-soluble drugs. Chem. Pharm. Bull. 1989, 37, 1404–1406. [Google Scholar] [CrossRef] [PubMed]
  111. Intarakumhaeng, R.; Wanasathop, A.; Li, K. Effects of solvents on skin absorption of nonvolatile lipophilic and polar solutes under finite dose conditions. Int. J. Pharm. 2018, 536, 405–413. [Google Scholar] [CrossRef]
  112. Chaudhuri, S.R.; Gajjar, R.; Krantz, W.; Kasting, G. Percutaneous absorption of volatile solvents following transient liquid exposure II. Ethanol. Chem. Eng. Sci. 2009, 64, 1665–1672. [Google Scholar] [CrossRef]
  113. Kurihara–Bergstrom, T.; Knutson, K.; DeNoble, L.J.; Goates, C.Y. Percutaneous absorption enhancement of an ionic molecule by ethanol-water systems in human skin. Pharm. Res. 1990, 7, 762–766. [Google Scholar] [CrossRef] [PubMed]
  114. Matsumoto, M.; Todo, H.; Akiyama, T.; Hirata-Koizumi, M.; Sugibayashi, K.; Ikarashi, Y.; Ono, A.; Hirose, A.; Yokohama, K. Risk assessment of skin lightening cosmetics containing hydroquinone. Regul. Toxicol. Pharmacol. 2016, 81, 128–135. [Google Scholar] [CrossRef] [PubMed]
  115. Uchida, T.; Kadhum, W.R.; Kanai, S.; Todo, H.; Oshizaka, T.; Sugibayashi, K. Prediction of skin permeation by chemical compounds using the artificial membrane, Strat-M™. Eur. J. Pharm. Sci. 2015, 67, 113–118. [Google Scholar] [CrossRef] [PubMed]
  116. Arce, F.V.; Asano, N.; Yamashita, K.; Oda, A.; Uchida, T.; Sano, T.; Todo, H.; Sugibayashi, K. Effect of layered application on the skin permeation of a cosmetic active component, rhododendrol. J. Toxicol. Sci. 2019, 44, 1–11. [Google Scholar] [CrossRef] [PubMed]
  117. Santos, P.; Watkinson, A.C.; Hadgraft, J.; Lane, M.E. Oxybutynin permeation in skin: The influence of drug and solvent activity. Int. J. Pharm. 2010, 384, 67–72. [Google Scholar] [CrossRef] [PubMed]
  118. Gajjar, R.M.; Miller, M.A.; Kasting, G.B. Evaporation of volatile organic compounds from human skin in vitro. Ann. Occup. Hyg. 2013, 57, 853–865. [Google Scholar]
  119. Yamaguchi, M.; Araki, D.; Kanamori, T.; Okiyama, Y.; Seto, H.; Uda, M.; Usami, M.; Yamamoto, Y.; Masunaga, T.; Sasa, H. Actual consumption amount of personal care products reflecting Japanese cosmetic habits. J. Toxicol. Sci. 2017, 42, 797–814. [Google Scholar] [CrossRef] [Green Version]
  120. Ma, H.; Yu, M.; Tan, F.; Li, N. Improved percutaneous delivery of azelaic acid employing microemulsion as nanocarrier: Formulation optimization, in vitro and in vivo evaluation. RSC Adv. 2015, 5, 28985–28995. [Google Scholar] [CrossRef]
  121. Choi, Y.L.; Park, E.J.; Kim, E.; Na, D.H.; Shin, Y. Dermal stability and in vitro skin permeation of collagen pentapeptides (KTTS and palmitoyl-KTTS). Biomol. Ther. 2014, 22, 321–327. [Google Scholar]
  122. Schwarz, J.; Baisaeng, N.; Hoppel, M.; Löw, M. Ultra-small NLC for improved dermal delivery of coenzyme Q10. Int. J. Pharm. 2013, 447, 213–217. [Google Scholar] [CrossRef]
  123. Comiskey, D.; Api, A.M.; Baratt, C.; Daly, E.J.; Ellis, G.; McNamara, C.; O’Mahony, C.; Robinson, S.H.; Safford, B.; Smith, B.; et al. Novel database for exposure to fragrance ingredients in cosmetics and personal care products. Regul. Toxicol. Pharmacol. 2015, 72, 660–672. [Google Scholar] [CrossRef] [PubMed]
  124. Klimová, Z.; Hojerová, J.; Beránková, M. Skin absorption and human exposure estimation of three widely discussed UV filters in sunscreens–In vitro study mimicking real-life consumer habits. Food Chem. Toxicol. 2015, 83, 237–250. [Google Scholar] [CrossRef] [PubMed]
  125. Abe, A.; Saito, M.; Kadhum, W.R.; Todo, H.; Sugibayashi, K. Establishment of an evaluation method to detect drug disposition in hair follicles. Int. J. Pharm. 2018, 542, 27–35. [Google Scholar] [CrossRef] [PubMed]
  126. Widyaninggar, A.; Triyana, K.; Rohman, A. Differentiation between porcine and bovine gelatin in capsule shells based on amino acid profiles and principal component analysis. Indones. J. Pharm. 2012, 23, 104–109. [Google Scholar]
  127. Rohman, A.; Che Man, Y.B. Analysis of pig derivatives for halal authentication studies. Food Rev. Int. 2012, 28, 97–112. [Google Scholar] [CrossRef]
  128. Nemati, M.; Oveisi, M.R.; Abdollahi, H.; Sabzevari, O. Differentiation of bovine and porcine gelatins using principal component analysis. J. Pharm. Biomed. Anal. 2004, 34, 485–492. [Google Scholar] [CrossRef]
  129. Zhang, G.; Liu, T.; Wang, Q.; Chen, L.; Lei, J.; Luo, J.; Ma, G.; Su, Z. Mass spectrometric detection of marker peptides in tryptic digests of gelatin: A new method to differentiate between bovine and porcine gelatin. Food Hydrocoll. 2009, 23, 2001–2007. [Google Scholar] [CrossRef]
  130. Cheng, X.L.; Wei, F.; Xiao, X.Y.; Zhao, Y.Y.; Shi, Y.; Liu, W.; Zhang, P.; Ma, S.C.; Tian, S.S.; Lin, R.C. Identification of five gelatins by ultra performance liquid chromatography/time-of-flight mass spectrometry (UPLC/Q-TOF-MS) using principal component analysis. J. Pharm. Biomed. Anal. 2012, 62, 191–195. [Google Scholar] [CrossRef] [PubMed]
  131. Yilmaz, M.T.; Kesmen, Z.; Baykal, B.; Sagdic, O.; Kulen, O.; Kacar, O.; Yetim, H.; Baykal, A.T. A novel method to differentiate bovine and porcine gelatins in food products: NanoUPLC-ESI-Q-TOF-MSE based data independent acquisition technique to detect marker peptides in gelatin. Food Chem. 2013, 141, 2450–2458. [Google Scholar] [CrossRef] [PubMed]
  132. Sha, X.M.; Zhang, L.J.; Tu, Z.C.; Zhang, L.Z.; Hu, Z.Z.; Li, Z.; Li, X.; Huang, T.; Wang, H.; Zhang, L.; et al. The identification of three mammalian gelatins by liquid chromatography-high resolution mass spectrometry. LWT Food Sci. Technol. 2018, 89, 74–86. [Google Scholar] [CrossRef]
  133. Jumhawan, U.; Xing, J.; Zhan, Z. Detection and Differentiation of Bovine and Porcine Gelatins in Food and Pharmaceutical Products by LC/MS/MS Method. Shimadzu Application News No. AD-0164. 2017. Available online: https://www.ssi.shimadzu.com/sites/ssi.shimadzu.com/files/bovine-and-porcine-gelatins.pdf (accessed on 5 January 2019).
  134. Che Man, Y.B.; Syahariza, Z.A.; Mirghani, M.E.S.; Jinap, S.; Bakar, J. Analysis of potential lard adulteration in chocolate and chocolate products using Fourier transform infrared spectroscopy. Food Chem. 2005, 90, 815–819. [Google Scholar] [CrossRef]
  135. Nikzad, J.; Shahhosseini, S.; Tabarzad, M.; Nafissi-Varcheh, N.; Torshabi, M. Simultaneous detection of bovine and porcine DNA in pharmaceutical gelatin capsules by duplex PCR assay for halal authentication. DARU J. Pharm. Sci. 2017, 25, 1–11. [Google Scholar] [CrossRef] [PubMed]
  136. Sultana, S.; Motalib Hossain, M.A.; Nizar, N.N.A.; Eaqub Ali, M. Novel multiplex PCR-RFLP assay discriminates bovine, porcine and fish gelatin substitution in Asian pharmaceuticals capsule shell. Food Addit. Contam. Part A 2018, 35, 1662–1673. [Google Scholar] [CrossRef] [PubMed]
  137. Nur Azira, T.; Amin, I.; Che Man, Y.B. Differentiation of bovine and porcine gelatins in processed products via sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and principal component analysis (PCA) techniques. Int. Food Res. J. 2012, 19, 1175–1180. [Google Scholar]
  138. Hidaka, S.; Liu, S.Y. Effects of gelatins on calcium phosphate precipitation: A possible application for distinguishing bovine bone gelatin from porcine skin gelatin. J. Food Compos. Anal. 2003, 16, 477–483. [Google Scholar] [CrossRef]
Table 1. Halal cosmetic ingredients.
Table 1. Halal cosmetic ingredients.
CategoryExamplesReferences
Skin whitening agents4-potassium methoxysalicylate (4-MSK)[9,10]
Arbutin[11,12]
Ferulic acid[13]
Hinokitol[14]
Kojic acid[15,16]
Resveratrol[17]
Tranexamic acid [18]
Vitamin B3[19]
Vitamin C[20]
Anti-aging agentsCapsanthin[21]
Capsorubin[21]
Delphinidin[22]
Gallic acid[23]
Genistein[24]
Glycyrrhizin[25]
Lutein[26]
Phloretin[27]
Salidroside[28]
Sclareol[29]
Trans-communic acid (TCA)[30]
Umbelliferone[31]
Vitamin B3[19]
ThickenersCarboxymethyl cellulose[32]
Carnauba wax[33]
Carrageenan[34]
Petrolatum[35]
ColorantsCarotene (red-orange)[7,36]
Lithospermum purple (violet)[7,36]
Paprika (yellow, orange, red)[7,36]
Safflower (yellow, red)[7,36]
Turmeric (yellow)[7,36]
SolventsAvocado oil[37,38]
Corn oil[39]
Cottonseed oil[40]
Dipropylene glycol[41]
Jojoba oil[42]
Liquid paraffin (mineral oil)[43,44]
Polyethylene glycol[45]
Safflower oil[46]
Sesame oil[47]
Water[4]
Table 2. Haram cosmetic ingredients.
Table 2. Haram cosmetic ingredients.
CategoryExamplesReferences
Restricted chemicalsChlorofluorocarbon propellants[48]
Chloroform[48]
Halogenated salicylanilides[48]
Hexachlorophene[48]
Mercury compounds[48]
Methylene chloride[48]
Prohibited cattle materials[48]
Vinyl chloride[48]
Zirconium-containing complexes[48]
Insect derivedCarmine dye (Cochineal; E 120 or Natural Red 4)[7,36]
Crimson dye (from Kermes vermilio)[7,36]
Laccaic acid [7,36]
Beeswax[49]
Human derivedAmniotic fluid[4]
Growth factors[4]
Placenta[4]
Porcine derivedAmniotic fluid[4,50]
Gelatin[4]
Growth factors[4,50]
Placenta[4,50]
Table 3. Critical cosmetic ingredients.
Table 3. Critical cosmetic ingredients.
CategoryIngredientsCommentsReferences
ActivesAllantoinMay be derived from unspecified animal urine [52]
Alpha hydroxy acidsMay be derived from unspecified animals[53,54]
Azelaic acidMay be derived from oleic acid of unspecified animal origin; haram if contaminated with Malassezia furfur[55]
Caffeic acidMay be synthesized using microbes or obtained from bee propolis; Halal if plant-derived[56,57]
CollagenMay be porcine-derived, human-derived; halal if marine-derived[58]
Hyaluronic acidMay be derived from unspecified animal tissues[59]
KeratinMay be derived from cashmere goat or sheep wool[4,60,61]
MequinolMay be synthesized using methanol[62]
OligopeptidesMay be derived from unspecified microorganisms and animals[63]
Ubiquinone (CoQ10)May be derived from unspecified animals[64,65]
UreaMay be derived from unspecified animals[4,66]
Vitamin EMay be produced from non-halal processes (i.e., use of lipase or unspecified origin of precursor materials) [67]
ThickenersGelatinMay be porcine-derived; halal if derived from fish[68]
Palmitic acidMay be derived from unspecified animals; halal if plant-derived[69]
Xanthan gumHaram if contaminated with fermenting bacterium; halal if uncontaminated and obtained from natural aerobic fermentation [70]
OilsLinoleic acid/Linolenic acidMay be derived from unspecified animals; halal if plant-derived[71]
Oleic acidMay be porcine-derived[72]
Palm kernel oilMay be derived from unspecified animals[73]
Stearic acid/stearyl alcoholMay be porcine-derived; halal if plant-derived[74]
SqualaneMay be derived from unspecified animals; halal if plant-derived [75]
WaxesCetyl alcoholMay be derived from palmitic acid of unspecified animal origin[76,77,78]
Lanolin alcoholMay be derived from non-halal slaughtered animals; halal if obtained from living animals[79]
Stearyl alcoholMay be derived from stearic acid of unspecified animal origin[74]
SolventsEthanolMust be from natural aerobic fermentation or synthetic ethanol; intended as preservative in cosmetic formulations [51,80]
Glycerin/glycerolMay be porcine-derived[81]
Propylene glycolMay be derived from glycerol of unspecified animal origin [82,83]
Table 4. List of guidelines for cosmetic production.
Table 4. List of guidelines for cosmetic production.
GuidelinesDescriptionReferences
ISO 22716:2007Good Manufacturing Practices (GMP) Guidelines for Cosmetics[84]
OIC/SMIIC 4:2018Standard and Metrology Institute for the Islamic Countries—Halal Cosmetics Requirements [85]
GSO 2055-4:2014Gulf Cooperation Council Standardization Organization (GSO)—Requirements for Cosmetics and Personal Care [86]
LPPOM MUI: HAS23000:1MUI Halal Certification Requirements[87]
ASEAN Cosmetic DirectivesAssociation for South East Asian Nations Guiding Document for Cosmetic Manufacturers and Consumers[88]
MS 2200-1:2008Islamic Consumer Goods Part 1: Cosmetic and Personal Care-General Guidelines[89]
NPRA Guidelines: 2017Guidelines for Control of Cosmetic Products in Malaysia[90]
U.S. FDA Guidance for IndustryCosmetic Good Manufacturing Practices[91]
ICH Guidelines Q7: 2016International Council for Harmonization Guidelines on Good Manufacturing Practices[92]
Table 5. Points for consideration in halal assurance system.
Table 5. Points for consideration in halal assurance system.
a. Comprehensive document exhibiting halal assurance system
b. Comprehensive material specification used in the production of halal cosmetics
c. Comprehensive and valid halal certification of materials and facility
d. Compliance of formulation ingredients and the list of halal materials
e. Conformity between material purchasing document and the list of halal material
f. Comprehensive document and conformity between production document and the list of halal materials
g. Comprehensive document and conformity between warehousing/storage document and list of halal materials and products
h. Traceability system
Table 6. List of methods used in the quantification of cosmetic ingredients.
Table 6. List of methods used in the quantification of cosmetic ingredients.
IngredientsAnalytical technique References
Azelaic acidHigh-performance liquid chromatography (215 nm, acetonitrile:phosphate buffer; 25:75 (v/v))[120]
Collagen, pentapeptideLiquid chromatography–tandem mass spectroscopy (Pentafluoropropionic acid solution:acetonitrile; 87:13 (v/v))[121]
Ethanol (14C-ethanol)Liquid scintillation counting [112]
Glycerin (14C-glycerol)Liquid scintillation counting[111]
Propylene glycolGas chromatography (helium as carrier gas)[117]
Ubiquinone (CoQ10)UV-Vis spectroscopy (405 nm)[122]
Urea (14C-urea)Liquid scintillation counting[111]

Share and Cite

MDPI and ACS Style

Sugibayashi, K.; Yusuf, E.; Todo, H.; Dahlizar, S.; Sakdiset, P.; Arce, F.J.; See, G.L. Halal Cosmetics: A Review on Ingredients, Production, and Testing Methods. Cosmetics 2019, 6, 37. https://0-doi-org.brum.beds.ac.uk/10.3390/cosmetics6030037

AMA Style

Sugibayashi K, Yusuf E, Todo H, Dahlizar S, Sakdiset P, Arce FJ, See GL. Halal Cosmetics: A Review on Ingredients, Production, and Testing Methods. Cosmetics. 2019; 6(3):37. https://0-doi-org.brum.beds.ac.uk/10.3390/cosmetics6030037

Chicago/Turabian Style

Sugibayashi, Kenji, Eddy Yusuf, Hiroaki Todo, Sabrina Dahlizar, Pajaree Sakdiset, Florencio Jr Arce, and Gerard Lee See. 2019. "Halal Cosmetics: A Review on Ingredients, Production, and Testing Methods" Cosmetics 6, no. 3: 37. https://0-doi-org.brum.beds.ac.uk/10.3390/cosmetics6030037

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop