Stabilization of Oxidation Prone Ingredients
Stabilization of Oxidation Prone Ingredients
by Sarah Taylor, PharmD
One of
the constant struggles compounding pharmacists face is the stabilization of
ingredients and formulations that are subject to change depending on a
patient’s specific needs and conditions. Compatibility of different individual
ingredients and combinations of ingredients at a wide potential range of
concentrations can be difficult to ascertain without trial, error, and
observation in the lab. In this newsletter, we will discuss a few active
pharmaceutical ingredients (APIs) that often cause issues and review
stabilizers that can be added that have demonstrated efficacy for reducing
oxidation.
Some ingredients
commonly used for hyperpigmentation or other cosmetic conditions, such as aging
skin are prone to oxidative degradation. Common examples include hydroquinone,
kojic acid, and tretinoin.1 The degradation of hydroquinone and
kojic acid is associated with a darkening of color usually to a yellowish or
brownish hue that is easily visually detectable.2,3 Tretinoin is
also susceptible to degradation by oxidation.4 The bulk powder
itself is already a yellow color, and unlike with kojic acid and hydroquinone,
significant color change may not be observed in association with degradation of
tretinoin.
Interventions
such as preventing prolonged exposure to light can help to prevent oxidation
and degradation of these APIs.4 We should also consider the addition
of chemicals called antioxidants to help prevent degradation of these APIs. Antioxidants
work to prevent free radicals, which are atoms, molecules, or ions with
unpaired electrons, from causing oxidation that, in the context of
pharmaceuticals, can result in rapid drug degradation or generation of unwanted
metabolites.5 Common antioxidants include vitamin E, ascorbic acid,
ascorbyl palmitate, buylated hydroxyanisole (BHA), butylated hydroxytoluene
(BHT), citric acid, sodium metabisulfite, and sodium bisulfite among others. Choosing
an antioxidant or a series of antioxidants can be challenging. Properties to
consider when choosing an antioxidant include route of administration,
solubility of antioxidant and characteristics of the compounded preparation, as
well as APIs in question.
Some antioxidants
such as BHA, BHT, and vitamin E have solubility in organic solvents such as
ethanol, and propylene glycol or solubility in oils. These antioxidants are
part of a group of antioxidants referred to as phenolic antioxidants and are
commonly used in anhydrous preparations consisting of organic solvents or oils.6
Ascorbyl palmitate, a partially lipid soluble form of ascorbic acid, also has
solubility in organic solvents. Bisulfites including sodium metabisulfite and
sodium bisulfite, in addition to citric acid, and ascorbic acid are all soluble
in aqueous environments and are commonly used as antioxidants in aqueous based
preparations such as creams, gels, or solutions.6 In aqueous
environments, pH can play a factor in activity of a given antioxidant, for
example, sodium metabisulfite has greater activity at pH in the acidic range
and can undergo autoxidation if exposed to elevated pH, whereas BHA is stable
up to a pH of 9.7 In addition to solubility and pH, another factor
to consider is how your antioxidants work together, for example, vitamin E and ascorbyl
palmitate are often used together due to a synergistic effect improving their
antioxidant capabilities. Oftentimes, a combination of antioxidants are used
together in compounded topical preparations to stabilize our oxidation prone
ingredients.
There
are many factors that affect which antioxidant is best for a given preparation
including route of administration, API we intend to stabilize, and chemical and
physical characteristics of the vehicle. To help you organize this material, Fagron
Academy has put together a chart you can click
here to view
that offers a summary of a few common antioxidants, which routes they are
typically used for, the concentration typically used, as well as information on
solubility and temperature stability.
Sources:
1.
Bandyopadhyay D. Topical treatment of
melasma. Indian J Dermatol. 2009;54(4):303-9. doi: 10.4103/0019-5154.57602.
2.
Enguita FJ, Leitão AL. Hydroquinone:
environmental pollution, toxicity, and microbial answers. Biomed Res Int.
2013;2013:542168. doi: 10.1155/2013/542168.
3.
Draelos Z, Yatskayer M, Bhushan P,
Pillai S, Oresaho C. Evaluation of kojic acid, emblica extract, and glycolic
acid formulation compared with hydroquinone 4% for skin lightening.
Therapeutics for the Clinician. 2010; 86: 153-158.
4.
Del Rosso JQ, Pillai R, Moore R.
Absence of Degradation of Tretinoin When Benzoyl Peroxide is Combined with an
Optimized Formulation of Tretinoin Gel (0.05%). J Clin Aesthet Dermatol.
2010;3(10):26-28.
5.
Lü JM, Lin PH, Yao Q, Chen C. Chemical
and molecular mechanisms of antioxidants: experimental approaches and model
systems. J Cell Mol Med. 2010;14(4):840-860.
doi:10.1111/j.1582-4934.2009.00897.x
6.
Musakhanian, J., Rodier, JD. &
Dave, M. Oxidative Stability in Lipid Formulations: a Review of the Mechanisms,
Drivers, and Inhibitors of Oxidation. AAPS PharmSciTech 23, 151 (2022). https://doi.org/10.1208/s12249-022-02282-0
7.
Rowe R, Sheskey P, Cook W, Fenton M.
Handbook of Pharmaceutical Excipients. Philadelphia, PA: Pharmaceutical Press.
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