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超临界二氧化碳作为一种绿色替代物用于实现药物与环糊精的络合。

Supercritical Carbon Dioxide as a Green Alternative to Achieve Drug Complexation with Cyclodextrins.

作者信息

Banchero Mauro

机构信息

Department of Applied Science and Technology, Politecnico di Torino, Corso Duca degli Abruzzi, 24, 10129 Torino, Italy.

出版信息

Pharmaceuticals (Basel). 2021 Jun 11;14(6):562. doi: 10.3390/ph14060562.

DOI:10.3390/ph14060562
PMID:34208286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8230899/
Abstract

Cyclodextrins are widely used in pharmaceutics to enhance the bioavailability of many drugs. Conventional drug/cyclodextrin complexation techniques suffer from many drawbacks, such as a high residual content of toxic solvents in the formulations, the degradation of heat labile drugs and the difficulty in controlling the size and morphology of the product particles. These can be overcome by supercritical fluid technology thanks to the outstanding properties of supercritical CO (scCO) such as its mild critical point, its tunable solvent power, and the absence of solvent residue after depressurization. In this work the use of scCO as an unconventional medium to achieve the complexation with native and substituted cyclodextrins of over 50 drugs, which belong to different classes, are reviewed. This can be achieved with different approaches such as the "supercritical solvent impregnation" and "particle-formation" techniques. The different techniques are discussed to point out how they affect the complexation mechanism and efficiency, the physical state of the drug as well as the particle size distribution and morphology, which finally condition the release kinetics and drug bioavailability. When applicable, the results obtained for the same drug with various cyclodextrins, or different complexation techniques are compared with those obtained with conventional approaches.

摘要

环糊精在制药领域被广泛用于提高多种药物的生物利用度。传统的药物/环糊精络合技术存在许多缺点,例如制剂中有毒溶剂残留量高、热不稳定药物降解以及难以控制产品颗粒的大小和形态。由于超临界CO₂(scCO₂)具有诸如温和的临界点、可调的溶剂能力以及减压后无溶剂残留等优异特性,超临界流体技术可以克服这些缺点。在这项工作中,综述了使用scCO₂作为非常规介质与50多种不同类别的药物的天然和取代环糊精实现络合的情况。这可以通过不同的方法实现,如“超临界溶剂浸渍”和“颗粒形成”技术。讨论了不同的技术,以指出它们如何影响络合机制和效率、药物的物理状态以及粒径分布和形态,这些最终决定了释放动力学和药物生物利用度。在适用的情况下,将用各种环糊精或不同络合技术对同一药物获得的结果与用传统方法获得的结果进行比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/d2f1b371960c/pharmaceuticals-14-00562-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/c7258671eced/pharmaceuticals-14-00562-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/f3c3660fd690/pharmaceuticals-14-00562-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/2c1842382815/pharmaceuticals-14-00562-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/3013849d183d/pharmaceuticals-14-00562-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/9084649a74a8/pharmaceuticals-14-00562-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/d2f1b371960c/pharmaceuticals-14-00562-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/c7258671eced/pharmaceuticals-14-00562-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/f3c3660fd690/pharmaceuticals-14-00562-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/2c1842382815/pharmaceuticals-14-00562-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/3013849d183d/pharmaceuticals-14-00562-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/9084649a74a8/pharmaceuticals-14-00562-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5fa/8230899/d2f1b371960c/pharmaceuticals-14-00562-g006.jpg

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