Advancements in Transdermal Drug Delivery: Nanoemulgels, Essential Oils, and Innovations in Colchicine Delivery for Improved Anti-Inflammatory Effects and Permeability Enhancement.

Iram Jahan, Atul Pratap Singh, Gaurav
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Abstract

Introduction: Transdermal drug delivery (TDD) systems offer a patient-friendly alternative to oral and injectable routes by enhancing bioavailability and bypassing hepatic first-pass metabolism. Nanoemulgels, which integrate nanoemulsions with gel matrices, provide improved drug solubilization, stability, and skin permeation. Incorporating both herbal components, such as Nigella sativa oil, and synthetic permeation enhancers, presents a synergistic strategy for enhancing the efficacy of anti-inflammatory agents like colchicine.

Methods: This review critically evaluates the formulation, pharmacological benefits, and permeation- enhancing strategies of nanoemulgels containing colchicine. Literature was selected from major scientific databases, emphasizing studies that investigated the combined effects of herbal and synthetic excipients on drug delivery and therapeutic performance.

Results: Evidence indicates that nanoemulgels incorporating Nigella sativa oil and pharmaceuticalgrade permeation enhancers significantly improve colchicine's dermal absorption, sustain drug release, and reduce systemic toxicity. The synergistic interaction between natural bioactives and synthetic agents enhances both anti-inflammatory activity and skin permeability.

Discussion: The dual role of Nigella sativa as an anti-inflammatory and natural permeation enhancer, when paired with synthetic excipients, demonstrates superior pharmacodynamic outcomes. This integrated approach enhances the therapeutic index of colchicine while minimizing adverse effects.

Conclusion: Combining herbal oils like Nigella sativa with pharmaceutical excipients in nanoemulgel systems represents a robust strategy for transdermal delivery. This platform improves drug penetration, stabilizes formulation performance, and amplifies therapeutic efficacy, offering a transformative alternative for chronic inflammatory conditions such as gout.

经皮给药的进展:纳米凝胶、精油和秋水仙碱给药的创新,以改善抗炎作用和增强渗透性。
简介:经皮给药(TDD)系统通过提高生物利用度和绕过肝脏第一过代谢,为口服和注射途径提供了一种对患者友好的替代方案。纳米乳剂将纳米乳剂与凝胶基质结合在一起,可以改善药物的增溶性、稳定性和皮肤渗透性。结合这两种草药成分,如黑草油和合成渗透增强剂,提出了一种协同策略,以提高抗炎剂如秋水仙碱的功效。方法:本文综述了秋水仙碱纳米凝胶的配方、药理作用和渗透增强策略。文献选择主要的科学数据库,重点研究草药和合成辅料对药物传递和治疗效果的联合作用。结果:有证据表明,含有黑草油和药用级渗透促进剂的纳米凝胶可显著改善秋水仙碱的皮肤吸收,维持药物释放,降低全身毒性。天然生物活性与合成制剂之间的协同作用增强了抗炎活性和皮肤渗透性。讨论:黑草作为抗炎和天然渗透促进剂的双重作用,当与合成赋形剂配对时,显示出优越的药效学结果。这种综合方法提高了秋水仙碱的治疗指标,同时最大限度地减少了不良反应。结论:在纳米凝胶系统中结合黑皮草等草药油和药用辅料是一种有效的透皮给药策略。该平台提高了药物渗透,稳定了配方性能,并扩大了治疗效果,为痛风等慢性炎症疾病提供了一种变革性的替代方案。
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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