Targeted drug delivery to the lungs using mesoporous silica nanoparticles

Nagashubha Bobbarjang, Praveena Kasi, Charitha Bandlapalli, Madhu Repollu Maddileti, Padmanabha Reddy Y, Kiran Sai Maccha
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Abstract

Delivering drugs to tumour or defective cells effectively and efficiently while minimizing harmful side effects is one of the biggest issues facing the medical field. In order to address this issue, the pharmaceutical industry has developed a number of drug carriers that aid in getting the therapeutic medication or gene to the intended location. It has been discovered that mesoporous silica nanoparticles are biocompatible, chemically and thermally stable nanoparticles for this purpose the amount of research on MSNs has increased significantly in the last few years. Since 2001, when MCM-41 was first suggested as a drug carrier for a controlled delivery system, followed by SBA-15 and MCM-48. When changed, morphological features like pore size, pore volume, particle size, surface area, pH, and drug loading capacity have a significant impact on MSNs. Drug distribution to the intended place is elaborated by functionalizing MSNs with organic and inorganic groups. The most recent studies on MSN synthesis techniques and its uses in medical imaging, diagnostics, cellular uptake, target medication administration, cell tracing, and biosensing are also included in this review article.
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利用介孔二氧化硅纳米颗粒向肺部靶向给药
有效、高效地将药物输送到肿瘤细胞或有缺陷的细胞,同时最大限度地减少有害副作用,是医学领域面临的最大问题之一。为了解决这个问题,制药业开发了许多药物载体,帮助将治疗药物或基因送到预定位置。人们发现,介孔二氧化硅纳米粒子是一种生物相容性好、化学性质和热稳定性高的纳米粒子。2001 年,MCM-41 首次被建议作为药物载体用于可控递送系统,随后,SBA-15 和 MCM-48 相继问世。当形态特征发生变化时,如孔径、孔容、粒度、表面积、pH 值和药物负载能力等,都会对 MSN 产生重大影响。通过用有机和无机基团对 MSN 进行功能化,可将药物分布到预定位置。本综述文章还介绍了有关 MSN 合成技术及其在医学成像、诊断、细胞摄取、靶向给药、细胞追踪和生物传感方面应用的最新研究。
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