A systemic review on development of mesoporous nanoparticles as a vehicle for transdermal drug delivery.

Q1 Pharmacology, Toxicology and Pharmaceutics
Praveen Kolimi, Sagar Narala, Ahmed Adel Ali Youssef, Dinesh Nyavanandi, Narendar Dudhipala
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引用次数: 0

Abstract

Recent advances in drug delivery technologies utilizing a variety of carriers have resulted in a paradigm shift in the current approach to diagnosis and therapy. Mesoporous silica nanoparticles (MSNs) were developed in response to the need for materials with high thermal, chemical, and mechanical properties. The synthesis, ease of surface functionalization, tunable pore size, large surface area, and biocompatibility of MSNs make them useful in a variety of biomedical applications such as drug delivery, theranostics, and stem cell research. In addition, MSNs have a high capability of delivering actives ranging from small molecules such as drugs and amino acids to larger peptides, vaccines, and antibodies in general. Moreover, MSN-based transdermal delivery has sparked a lot of interest because of the increase in drug stability, permeation, and ease of functionalization. The functionalization of MSNs plays an important role in the efficient delivery of therapeutic agents in a highly controlled manner. This review introduced dermal and transdermal drug delivery systems, explained the anatomy of the skin, and summarized different barriers that affect the transdermal delivery of many therapeutic agents. In addition, the fundamentals of MSNs together with their physicochemical properties, synthesis approaches, raw materials used in their fabrication, and factors affecting their physicochemical properties will be covered. Moreover, the applications of MSNs in dermal and transdermal delivery, the biocompatibility of MSNs in terms of toxicity and safety, and biodistribution will be explained with the help of a detailed literature review. The review is covering the current and future perspectives of MSNs in the pharmaceutical field with therapeutic applications.

介孔纳米颗粒作为透皮给药载体的开发系统综述。
近年来,利用各种载体的给药技术不断进步,导致目前的诊断和治疗方法发生了范式转变。介孔二氧化硅纳米颗粒(MSNs)是为满足对具有高热、化学和机械性能的材料的需求而开发的。MSNs 易于合成、表面功能化、孔径可调、比表面积大、生物相容性好,因此可用于多种生物医学应用,如药物输送、治疗学和干细胞研究。此外,MSN 还具有很强的递送活性,从药物和氨基酸等小分子到较大的肽、疫苗和一般抗体。此外,基于 MSN 的透皮给药因其提高药物稳定性、渗透性和易于功能化而引发了广泛的兴趣。MSN 的功能化在以高度可控的方式高效递送治疗药物方面发挥着重要作用。本综述介绍了皮肤和透皮给药系统,解释了皮肤的解剖结构,并总结了影响多种治疗药物透皮给药的不同障碍。此外,还将介绍 MSN 的基本原理、理化性质、合成方法、制造 MSN 的原材料以及影响其理化性质的因素。此外,还将借助详细的文献综述,解释 MSN 在皮肤和透皮给药方面的应用、MSN 在毒性和安全性方面的生物相容性以及生物分布。该综述涵盖了 MSN 在制药领域治疗应用的当前和未来前景。
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
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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