Pilot Study Demonstrates Tetramethylhexadecenyl Succinoyl Cysteine (TSC) Reduces Tretinoin-Induced Erythema and Dryness in Human Subjects

IF 2.3 4区 医学 Q2 DERMATOLOGY
Eduardo Pérez, José R. Fernández, Yasanuri Sato, Corey Fitzgerald, Karl Rouzard, Jason Healy, Masanori Tamura, Jeffry B. Stock, Tsuyoshi Ishii
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Abstract

Isoprenylcysteine (IPC) molecules represent a novel, safe class of compounds with a broad range of anti-inflammatory, antimicrobial, wound healing, and moisturizing properties. These molecules are primarily synthesized with two distinct long tail fatty acid chains attached to a cysteine residue, either possessing a 15-carbon farnesyl or a 20-carbon phytyl moiety. We previously reported that novel IPC compounds, diosodium tetramethylhexadecenyl succinoyl cysteine (TSC aka SIG1273) and acetylglutaminoyl farnesylcysteine (QFC aka SIG1191), possess several skin-protecting properties, including the inhibition of UVA, UVB, Ni+2, toll-like receptor, and T-cell receptor-induced inflammation [1-3]. Moreover, other farnesyl cysteine derivatives have been shown to reduce erythema when topically applied to human subjects [4], while phytyl cysteine–derived compounds have been shown to be well tolerated and reduce signs of aging and are effective in subjects with acne-prone skin [5, 6]. Topical retinoids, such as all-trans retinoic acid (tretinoin) and retinol, are commonly utilized in both the prescription and cosmetic space to treat acne and skin aging. Per Verified Market Reports, the global market size for tretinoin is currently valued at USD $7.64 billion and projected to surpass $10 billion by 2030. However, despite their effectiveness, the topical use of retinoids can cause burning, itching, stinging, and redness for consumers. Given their previous skin health–promoting activities, we sought to perform a pilot clinical study to assess whether TSC and/or QFC could effectively reduce tretinoin-induced irritation and thus ameliorate the negative side effects that come with its use.

This study was a 5-day efficacy evaluation with five subjects performed at a third party CRO (Validated Claim Support, Teaneck, NJ). There were four female and one male participant with a mean age of 35 years ranging from 31 to 42 years. No adverse events were observed. Four test sites on the subjects' backs were utilized: Test site 1—negative control (untreated), Test site 2—positive control (tretinoin 0.2%), Test site 3—(0.5% TSC + 0.2% tretinoin), and Test site 4—(0.5% QFC + 0.2% tretinoin). In addition to the actives, the only other ingredients used in each formulation were isopropyl palmitate (74.3%–74.8%) and pentylene glycol (25%). Test samples (0.1 mL) were applied topically under an occlusive patch at Days 0 and 1. No application was made on Days 3 or 4. Objective tolerance grading and clinical photography were captured from Day 1 to 4. Clinical results demonstrate that 0.5% TSC +0.2% tretinoin elicited a milder response and faster reduction in both dryness and erythema as compared to the positive control, tretinoin 0.2%, and 0.5% QFC + 0.2% tretinoin (Table 1; Figure 1). Increase in dryness persisted through the final evaluation day (Day 4) for the positive control, while 0.5% TSC + 0.2% tretinoin showed a decrease over the evaluation period (Table 1; Figure 1). A difference of 47% (mean cumulative scores) between 0.5% TSC + 0.2% tretinoin and tretinoin 0.2% was noted for dryness. Additionally, erythema in the 0.5% TSC + 0.2% tretinoin test site was reduced significantly by 68% (p = 0.010*) at Day 4 compared to tretinoin 0.2% (39%) and 0.5% QFC + 0.2% tretinoin (36%). The results from this pilot study suggest that the phytyl-cysteine lipid tail (TSC) may be more effective in reducing tretinoin-induced dryness and erythema than the farnesyl moiety, as QFC appeared to have little to no effect on this type of irritation, while TSC effectively improved dryness and reduced redness. Altogether, given these initial encouraging results, further study of TSC in a dose-dependent manner in a larger, controlled study is warranted.

E.P., J.S., Y.S., and J.F. designed the research study; T.I., K.R., C.F., Y.S., M.S., and E.P. analyzed the data; J.H. and M.T. contributed essential reagents or tools; and E.P. wrote the paper. All authors read and approved the final letter prior to submission.

This study was conducted in accordance with the intent and purpose of Good Clinical Practice regulations described in Title 21 of the U.S. Code of Federal Regulations (CFR) and the Declaration of Helsinki and its later amendments.

All authors of this letter are paid employees or consultants of Signum Biosciences or Rohto Pharmaceutical, which funded the study.

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来源期刊
CiteScore
4.30
自引率
13.00%
发文量
818
审稿时长
>12 weeks
期刊介绍: The Journal of Cosmetic Dermatology publishes high quality, peer-reviewed articles on all aspects of cosmetic dermatology with the aim to foster the highest standards of patient care in cosmetic dermatology. Published quarterly, the Journal of Cosmetic Dermatology facilitates continuing professional development and provides a forum for the exchange of scientific research and innovative techniques. The scope of coverage includes, but will not be limited to: healthy skin; skin maintenance; ageing skin; photodamage and photoprotection; rejuvenation; biochemistry, endocrinology and neuroimmunology of healthy skin; imaging; skin measurement; quality of life; skin types; sensitive skin; rosacea and acne; sebum; sweat; fat; phlebology; hair conservation, restoration and removal; nails and nail surgery; pigment; psychological and medicolegal issues; retinoids; cosmetic chemistry; dermopharmacy; cosmeceuticals; toiletries; striae; cellulite; cosmetic dermatological surgery; blepharoplasty; liposuction; surgical complications; botulinum; fillers, peels and dermabrasion; local and tumescent anaesthesia; electrosurgery; lasers, including laser physics, laser research and safety, vascular lasers, pigment lasers, hair removal lasers, tattoo removal lasers, resurfacing lasers, dermal remodelling lasers and laser complications.
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