Natural amphiphilic co-polymers as sustainable nanocarriers for enhanced solubility of hydrophobic drugs.

IF 3.5 4区 医学 Q2 ENGINEERING, BIOMEDICAL
Avnish Kumar, Anurag Verma, Gulshan Rathore
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引用次数: 0

Abstract

A major barrier to effective therapy is the limited water solubility of many Biopharmaceutics Classification System (BCS) Class II and IV medications, which results in poor bioavailability and inconsistent patient outcomes. Better solubilization and stability are provided by traditional synthetic nanocarriers such as PLGA, poloxamers, and PEG-PLA; however, these have disadvantages such as toxicity, cost, reliance on petrochemical resources, and regulatory barriers. Natural amphiphilic co-polymers (NACPs) are a sustainable and amiable alternative to proteins, polysaccharides, and phospholipids. Because of their innate amphiphilicity, which promotes self-assembly into micelles, vesicles, nanogels, and hydrogels, hydrophobic drugs can be effectively encapsulated and released under controlled conditions.This review focuses on the structural foundations of amphiphilicity in graft and block copolymers, naturally occurring self-assembling systems, and chemically modified derivatives that enhance solubility and drug-polymer interactions. In contrast to synthetic carriers, NACPs have other benefits such as mucoadhesion, enzymatic degradability, pH/enzyme responsiveness, and generally recognized as safe (GRAS) regulatory status, even though problems with scalability, reproducibility, and long-term stability still exist. Their versatility includes oral, parenteral, transdermal, pulmonary, nasal, and ocular drug delivery, with notable improvements in solubility, bioavailability, and therapeutic accuracy. Recent advancements include stimuli-responsive designs, hybrid natural-synthetic systems, and artificial intelligence (AI)-driven modeling for predicting drug-polymer compatibility. Collectively, NACPs present a sustainable strategy for next-generation nanomedicine that strikes a balance between therapeutic efficacy and environmental responsibility. By addressing solubility concerns with environmentally acceptable carriers, NACPs have a substantial translational potential to promote pharmaceutical innovation and green drug delivery systems.

天然两亲共聚物作为增强疏水药物溶解度的可持续纳米载体。
有效治疗的主要障碍是许多生物制药分类系统(BCS) II类和IV类药物的水溶性有限,这导致生物利用度差和患者预后不一致。传统的合成纳米载体如PLGA、poloxamers和PEG-PLA提供了更好的增溶性和稳定性;然而,这些方法存在毒性、成本、对石化资源的依赖以及监管障碍等缺点。天然两亲共聚物(NACPs)是一种可持续的、友好的蛋白质、多糖和磷脂的替代品。由于疏水药物具有天生的两亲性,可以促进自组装成胶束、囊泡、纳米凝胶和水凝胶,因此疏水药物可以在受控条件下被有效地封装和释放。本文综述了接枝共聚物和嵌段共聚物两亲性的结构基础,自然形成的自组装体系,以及增强溶解度和药物-聚合物相互作用的化学修饰衍生物。与合成载体相比,NACPs还有其他优点,如黏附性、酶降解性、pH/酶响应性,以及公认的安全(GRAS)监管状态,尽管存在可扩展性、可重复性和长期稳定性方面的问题。它们的用途广泛,包括口服、肠外、透皮、肺、鼻和眼给药,具有显著的溶解度、生物利用度和治疗准确性。最近的进展包括刺激响应设计、混合天然合成系统以及用于预测药物-聚合物相容性的人工智能(AI)驱动建模。总的来说,NACPs为下一代纳米医学提供了一个可持续的战略,在治疗效果和环境责任之间取得平衡。通过解决环境可接受载体的溶解度问题,NACPs具有促进制药创新和绿色给药系统的巨大转化潜力。
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
Journal of Biomaterials Science, Polymer Edition
Journal of Biomaterials Science, Polymer Edition 工程技术-材料科学:生物材料
CiteScore
7.10
自引率
5.60%
发文量
117
审稿时长
1.5 months
期刊介绍: The Journal of Biomaterials Science, Polymer Edition publishes fundamental research on the properties of polymeric biomaterials and the mechanisms of interaction between such biomaterials and living organisms, with special emphasis on the molecular and cellular levels. The scope of the journal includes polymers for drug delivery, tissue engineering, large molecules in living organisms like DNA, proteins and more. As such, the Journal of Biomaterials Science, Polymer Edition combines biomaterials applications in biomedical, pharmaceutical and biological fields.
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