Host-guest drug delivery by β-cyclodextrin assisted polysaccharide vehicles: A review

被引:38
|
作者
Sahu, Krishna Manjari [1 ]
Patra, Swapnita [1 ]
Swain, Sarat K. [1 ]
机构
[1] Veer Surendra Sai Univ Technol, Dept Chem, Sambalpur 768018, Odisha, India
关键词
Drug delivery; beta-Cyclodextrin; Polysaccharide; Host; -guest; Inclusion complex; GRAFTED CHITOSAN NANOPARTICLES; GUAR GUM; CONTROLLED-RELEASE; INCLUSION COMPLEX; HYALURONIC-ACID; CHITOSAN/CYCLODEXTRIN NANOPARTICLES; SUPRAMOLECULAR HYDROGELS; MOLECULAR ENCAPSULATOR; CELLULOSE; CARRIER;
D O I
10.1016/j.ijbiomac.2023.124338
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Among different forms of cyclodextrin (CD), beta-CD has been taken a special attraction in pharmaceutical science due to lowest aqueous solubility and adequate cavity size. beta-CD forms inclusion complex with drugs in combination with biopolymers such as polysaccharides which plays a vital role as a vehicle for safe release of drugs. It is noticed that, beta-CD assisted polysaccharide-based composite achieves better drug release rate through hostguest mechanism. Present review is a critical analysis of this host-guest mechanism for release of drugs from polysaccharide supported beta-CD inclusion complex. Various important polysaccharides such as cellulose, alginate, chitosan, dextran, etc. and their association with beta-CD in relevant to drug delivery are logically compared in present review. Efficacy of mechanism of drug delivery by different polysaccharides with beta-CD is analytically examined in schematic form. Drug release capacity at different pH conditions, mode of drug release, along with characterization techniques adopted by individual polysaccharide-based CD complexes are comparatively established in tabular form. This review may explore better visibility for researchers those are working in the area of controlled release of drugs by carrier consist of beta-CD associated polysaccharide composite through hostguest mechanism.
引用
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页数:20
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