Biocompatible Supramolecular Mesoporous Silica Nanoparticles as the Next-Generation Drug Delivery System

被引:15
|
作者
Mohamed, Farahidah [1 ]
Oo, May K. [1 ]
Chatterjee, Bappaditya [2 ]
Alallam, Batoul [3 ]
机构
[1] Int Islamic Univ Malaysia, Pharmaceut Technol Dept, Kulliyyah Pharm, Kuantan, Malaysia
[2] SVKMs Narsee Monjee Inst Management Studies, Shobhaben Pratapbhai Patel Sch Pharm & Technol Man, Mumbai, India
[3] Univ Sci Malaysia, Adv Med & Dent Inst, Cluster Integrat Med, George Town, Penang, Malaysia
关键词
mesoporous; silica; nanoparticles; insulin; pharmaceutical; oral; ANTICANCER DRUGS; CELLULAR UPTAKE; ORAL DELIVERY; RELEASE; SIZE; FORMULATION; SIRNA;
D O I
10.3389/fphar.2022.886981
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Supramolecular mesoporous silica nanoparticles (MSNs) offer distinct properties as opposed to micron-sized silica particles in terms of their crystal structure, morphology-porosity, toxicity, biological effects, and others. MSN biocompatibility has touched the pharmaceutical realm to exploit its robust synthesis pathway for delivery of various therapeutic molecules including macromolecules and small-molecule drugs. This article provides a brief review of MSN history followed by special emphasis on the influencing factors affecting morphology-porosity characteristics. Its applications as the next-generation drug delivery system (NGDDS) particularly in a controlled release dosage form via an oral drug delivery system are also presented and shall be highlighted as oral delivery is the most convenient route of drug administration with the economical cost of development through to scale-up for clinical trials and market launch.
引用
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页数:7
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