Cyclodextrin Based Host-Guest Inclusion Complex, an Approach to Enhancing the Physicochemical and Biopharmaceutical Application of Poorly Water-soluble Drugs

被引:5
作者
Inam, Muhammad [1 ,2 ,3 ]
Sareh Sadat, Moshirian-Farahi [4 ]
Chen, Wenjie [1 ,2 ,3 ,5 ]
机构
[1] Guangzhou Med Univ, Key Lab Mol Target & Clin Pharmacol, Guangzhou 511436, Peoples R China
[2] Guangzhou Med Univ, Sch Pharmaceut Sci, State & NMOA Key Lab Resp Dis, Guangzhou 511436, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 5, Guangzhou 511436, Peoples R China
[4] Islamic Azad Univ, Dept Appl Chem, Mashhad Branch, Mashhad, Iran
[5] Sydney Vital Translat Canc Res Ctr, Westbourne St, Sydney, NSW 2065, Australia
关键词
Poor water solubility; Inclusion complex; Physicochemical; Biopharmaceutical; BETA-CYCLODEXTRIN; SOLID DISPERSION; COCRYSTALS; POLYMER; RATS;
D O I
10.1007/s40242-023-3204-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Host-guest inclusion complexes have been extensively studied for drug delivery applications. The host molecule, typically cyclodextrin, creates a cavity, in which the guest molecule, such as a drug, can be encapsulated. This encapsulation can protect the drug from degradation, improve its solubility and stability, and enhance its bioavailability. Moreover, host-guest inclusion complexes can facilitate targeted drug delivery by selectively releasing drugs at the site of action. Various techniques, such as covalent bonding, non-covalent interactions, and self-assembly have been used to form these complexes. Host-guest inclusion complexes have shown great potential for improving the efficacy and safety of drug delivery systems. This mini review summarizes the application and recent progress of the cyclodextrin-based host-guest inclusion complex, highlighting the enhanced physicochemical and biopharmaceutical application of pharmaceutical drugs via formulation of its inclusion complex.
引用
收藏
页码:857 / 861
页数:5
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