Hydrophobic ion pairing with cationic derivatives of α-, ß-, and γ-cyclodextrin as a novel approach for development of a self-nano-emulsifying drug delivery system (SNEDDS) for oral delivery of heparin-Reference-Cited by-同舟云学术

Hydrophobic ion pairing with cationic derivatives of α-, ß-, and γ-cyclodextrin as a novel approach for development of a self-nano-emulsifying drug delivery system (SNEDDS) for oral delivery of heparin

Published:2021-11-02 Issue:11 Volume:47 Page:1809-1823
ISSN:0363-9045
Container-title:Drug Development and Industrial Pharmacy
language:en
Short-container-title:Drug Development and Industrial Pharmacy

Author:

Bahiraei Masoomeh¹,Derakhshandeh Katayoun¹²,Mahjub Reza¹²^ORCID

Affiliation:

1. Department of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran

2. Medicinal Plant and Natural Product Research Center, Hamadan, University of Medical Sciences, Hamadan, Iran

Funder

Deputy of Research and Technology, Hamadan University of Medical Sciences

Publisher

Informa UK Limited

Subject

Organic Chemistry,Drug Discovery,Pharmaceutical Science,Pharmacology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03639045.2022.2064485

Reference66 articles.

1. Delivery of LMW Heparin via Surface Coated Chitosan/peg-Alginate Microspheres Prevents Thrombosis

2. pH-responsive thiolated chitosan nanoparticles for oral low-molecular weight heparin delivery: in vitro and in vivo evaluation

3. Polycationic lipophilic-core dendrons as penetration enhancers for the oral administration of low molecular weight heparin

4. Encapsulation of low molecular weight heparins: Influence on the anti-Xa/anti-IIa ratio

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