用于肺部给药的核壳纳米颗粒

Q2 Pharmacology, Toxicology and Pharmaceutics
Mukesh P Ratnaparkhi, Shailendra S Salvankar, Avinash R Tekade, Gajanan M Kulkarni
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引用次数: 0

摘要

纳米级给药系统能够提高靶细胞内药物的细胞内浓度,从而提高疗效、减少剂量和与剂量相关的不良反应,因此在各种疗法中的应用引起了人们的兴趣。目前有多种类型的纳米颗粒,但核壳纳米颗粒在降低细胞毒性、高分散性和生物相容性方面优于裸纳米颗粒,而且由于具有更好的表面特性,可改善与药物和生物分子的结合。这些纳米颗粒给药系统可用于靶向结肠、大脑、肺部等多个器官。肺部给药是一种更有吸引力的方法,因为它是一种非侵入性的全身和局部给药途径,因为肺部具有广阔的表面积、脆弱的血肺泡屏障和显著的血管化。核壳纳米颗粒给药系统在治疗各种肺部疾病方面更为有效。因此,本综述讨论了几种核壳纳米粒子在治疗各种疾病方面的潜力以及核壳纳米粒子的合成方法。核壳纳米粒子的合成方法包括固相反应、液相反应、气相反应、机械混合、微波辅助合成、声波合成和非热等离子体技术。核壳纳米粒子的基本类型有金属核壳纳米粒子、磁性核壳纳米粒子、聚合物核壳纳米粒子、二氧化硅核壳纳米粒子、上转换核壳纳米粒子和碳纳米材料核壳纳米粒子。利用这种特殊的平台,可以综合芯壳材料和外壳材料的优点,如血清稳定性强、有效载药、粒径可调、免疫相容性好等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Core-Shell Nanoparticles for Pulmonary Drug Delivery.

Nanoscale drug delivery systems have provoked interest for application in various therapies on account of their ability to elevate the intracellular concentration of drugs inside target cells, which leads to an increase in efficacy, a decrease in dose, and dose-associated adverse effects. There are several types of nanoparticles available; however, core-shell nanoparticles outperform bare nanoparticles in terms of their reduced cytotoxicity, high dispersibility and biocompatibility, and improved conjugation with drugs and biomolecules because of better surface characteristics. These nanoparticulate drug delivery systems are used for targeting a number of organs, such as the colon, brain, lung, etc. Pulmonary administration of medicines is a more appealing method as it is a noninvasive route for systemic and locally acting drugs as the pulmonary region has a wide surface area, delicate blood-alveolar barrier, and significant vascularization. A core-shell nano-particulate drug delivery system is more effective in the treatment of various pulmonary disorders. Thus, this review has discussed the potential of several types of core-shell nanoparticles in treating various diseases and synthesis methods of core-shell nanoparticles. The methods for synthesis of core-shell nanoparticles include solid phase reaction, liquid phase reaction, gas phase reaction, mechanical mixing, microwave- assisted synthesis, sono-synthesis, and non-thermal plasma technology. The basic types of core-shell nanoparticles are metallic, magnetic, polymeric, silica, upconversion, and carbon nanomaterial- based core-shell nanoparticles. With this special platform, it is possible to integrate the benefits of both core and shell materials, such as strong serum stability, effective drug loading, adjustable particle size, and immunocompatibility.

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来源期刊
Pharmaceutical nanotechnology
Pharmaceutical nanotechnology Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.20
自引率
0.00%
发文量
46
期刊介绍: Pharmaceutical Nanotechnology publishes original manuscripts, full-length/mini reviews, thematic issues, rapid technical notes and commentaries that provide insights into the synthesis, characterisation and pharmaceutical (or diagnostic) application of materials at the nanoscale. The nanoscale is defined as a size range of below 1 µm. Scientific findings related to micro and macro systems with functionality residing within features defined at the nanoscale are also within the scope of the journal. Manuscripts detailing the synthesis, exhaustive characterisation, biological evaluation, clinical testing and/ or toxicological assessment of nanomaterials are of particular interest to the journal’s readership. Articles should be self contained, centred around a well founded hypothesis and should aim to showcase the pharmaceutical/ diagnostic implications of the nanotechnology approach. Manuscripts should aim, wherever possible, to demonstrate the in vivo impact of any nanotechnological intervention. As reducing a material to the nanoscale is capable of fundamentally altering the material’s properties, the journal’s readership is particularly interested in new characterisation techniques and the advanced properties that originate from this size reduction. Both bottom up and top down approaches to the realisation of nanomaterials lie within the scope of the journal.
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