Optimized Cutaneous Delivery of Anti-wrinkle Dipeptide KT via Molecular Modification: Preformulation, Permeation, and the Importance of Conjugate Chain Length

IF 2.2 4区 工程技术 Q3 PHARMACOLOGY & PHARMACY Bioimpacts Pub Date : 2023-07-18 DOI:10.34172/bi.2023.27558
Mahsa Sayed Tabatabaei, F. Kobarfard, R. Aboofazeli, Sorour Ramezanpour, H. Moghimi
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Abstract

Introduction: Anti-aging peptides, such as dipeptide KT, are promising rejuvenating agents and have recently received significant attention. However, their hydrophilic nature makes skin absorption therapeutically inadequate. The excessive hydrophilicity of peptides is partially solved by lipoidal conjugates, however, the increased molecular weight due to conjugation creates a new obstacle to skin permeation. Methods: In an attempt to concurrently solve these limitations, here we have studied different short-mid chain fatty acids (C6-C18) conjugates of dipeptide KT. Different fatty acid chain lengths of C6, C8, C10, C12, C14, C16, and C18 were considered to be conjugated with KT and screened in-silico. Of those, C8, C10, and C12 were preferred and synthesized alongside two controls of the parent drug (KT) and C16 (Pal-KT) as the commercialized form to be studied mechanistically. Subsequently, they were structurally characterized and underwent preformulation, supramolecular investigations (e.g., thermal behavior, solubility, surface-acting, crystalline structure), and skin absorption studies. Results: Data showed that the synthesized conjugates substantially outperformed Pal-KT in terms of molecular weight, lipophilicity, melting point, and aqueous solubility. In addition, unlike KT, they all demonstrated amphiphilicity-related features. The maximum and minimum skin permeation were assigned to C8-KT (33.2%) and KT (0.004%). Moreover, permeability coefficients (Kp) of the C8-KT, C10-KT, C12-KT, and C16-KT were calculated to be about 22000, 3800, 3400, and 1600 times higher than KT, respectively. Conclusion: Conjugate selection with lower molecular weight fatty acids and optimal lipophilicity can positively affect the molecular properties, skin absorption, and the ability to form supramolecular structures and consequently pave the way to ‘better’ anti-wrinkle products and formulations.
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通过分子修饰优化皱纹二肽KT的皮肤递送:预成型、渗透和共轭链长度的重要性
引言:抗衰老肽,如二肽KT,是一种很有前途的抗衰老剂,最近受到了极大的关注。然而,它们的亲水性使皮肤吸收治疗不足。肽的过度亲水性通过类脂缀合物部分解决,然而,由于缀合而增加的分子量对皮肤渗透造成了新的障碍。方法:为了同时解决这些限制,我们研究了二肽KT的不同短中链脂肪酸(C6-C18)偶联物。C6、C8、C10、C12、C14、C16和C18的不同脂肪酸链长被认为与KT偶联并在计算机上进行筛选。其中,C8、C10和C12是优选的,并与母体药物(KT)和C16(Pal-KT)的两个对照物一起合成,作为有待机制研究的商业化形式。随后,对它们进行了结构表征,并进行了预成型、超分子研究(如热行为、溶解度、表面作用、晶体结构)和皮肤吸收研究。结果:数据显示,合成的偶联物在分子量、亲脂性、熔点和水溶性方面显著优于Pal-KT。此外,与KT不同的是,它们都表现出了与两栖性相关的特征。最大和最小皮肤渗透分别为C8-KT(33.2%)和KT(0.004%)。此外,C8-KT、C10-KT、C12-KT和C16-KT的渗透系数(Kp)分别是KT的22000、3800、3400和1600倍。结论:低分子量脂肪酸和最佳亲脂性的结合物选择可以积极影响分子性质、皮肤吸收和形成超分子结构的能力,从而为“更好”的防皱产品和配方铺平道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Bioimpacts
Bioimpacts Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.80
自引率
7.70%
发文量
36
审稿时长
5 weeks
期刊介绍: BioImpacts (BI) is a peer-reviewed multidisciplinary international journal, covering original research articles, reviews, commentaries, hypotheses, methodologies, and visions/reflections dealing with all aspects of biological and biomedical researches at molecular, cellular, functional and translational dimensions.
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