Effects ofN-trimethyl chitosan chloride as an absorption enhancer on properties of insulin liquid suppository in vitro and in vivo

2005 ◽  
Vol 99 (3) ◽  
pp. 1140-1146 ◽  
Author(s):  
Wen He ◽  
Yumin Du ◽  
Wenbing Dai ◽  
Yan Wu ◽  
Mian Zhang
Keyword(s):  
Absorption Enhancer ◽  
Trimethyl Chitosan ◽  
Liquid Suppository

scholarly journals Improved In vivo Effect of Chrysin as an Absorption Enhancer Via the Preparation of Ternary Solid Dispersion with Brij®L4 and Aminoclay

2018 ◽  
Vol 16 (1) ◽  
pp. 86-92 ◽  
Author(s):  
Sang Hoon Lee ◽  
Yeo-song Lee ◽  
Jae Geun Song ◽  
Hyo-Kyung Han
Keyword(s):  
Drug Release ◽  
Drug Carrier ◽  
Solid Dispersions ◽  
Amorphous State ◽  
Absorption Enhancer ◽  
Cancer Resistance ◽  
Surface Acting ◽  
Strong Inhibitor

Background: Chrysin is a strong inhibitor of breast cancer resistance protein (BCRP) but it is practically insoluble in water. Effective solubilization of chrysin is critical for its pharmaceutical application as an absorption enhancer via inhibition of BCRP-mediated drug efflux. Objective: This study aimed to develop an effective oral formulation of chrysin to improve its in vivo effect as an absorption enhancer. Method: Solid dispersions (SDs) of chrysin were prepared with hydrophilic carriers having surface acting properties and a pH modulator. In vitro and in vivo characterizations were performed to select the optimal SDs of chrysin. Results: SDs with Brij&®L4 and aminoclay was most effective in increasing the solubility of chrysin by 13-53 fold at varying drug-carrier ratios. Furthermore, SDs significantly improved the dissolution rate and extent of drug release. SDs (chrysin: Brij&®L4: aminoclay=1:3:5) achieved approximately 60% and 83% drug release within 1 h and 8 h, respectively, in aqueous medium, while the dissolution of the untreated chrysin was less than 13%. XRD patterns indicated the amorphous state of chrysin in SDs. The SD formulation was effective in improving the bioavailability of topotecan, a BCRP substrate in rats. Following oral administration of topotecan with the SDs of chrysin, the Cmax and AUC of topotecan was enhanced by approximately 2.6- and 2-fold, respectively, while the untreated chrysin had no effect. Conclusion: The SD formulation of chrysin with Brij&®L4 and aminoclay appeared to be promising in improving the dissolution of chrysin and enhancing its in vivo effect as an absorption enhancer.

Enhancement of bronchial octreotide absorption by chitosan and N-trimethyl chitosan shows linear in vitro/in vivo correlation

2006 ◽  
Vol 110 (2) ◽  
pp. 353-361 ◽  
Author(s):  
Bogdan I. Florea ◽  
Maya Thanou ◽  
Hans E. Junginger ◽  
Gerrit Borchard
Keyword(s):  
Trimethyl Chitosan

In vitro and in vivo study of N-trimethyl chitosan nanoparticles for oral protein delivery

2008 ◽  
Vol 349 (1-2) ◽  
pp. 226-233 ◽  
Author(s):  
Fu Chen ◽  
Zhi-Rong Zhang ◽  
Fang Yuan ◽  
Xuan Qin ◽  
Minting Wang ◽  
...  
Keyword(s):  
Protein Delivery ◽  
Chitosan Nanoparticles ◽  
In Vivo Study ◽  
Trimethyl Chitosan ◽  
Oral Protein Delivery

Thiolated trimethyl chitosan nanocomplexes as gene carriers with high in vitro and in vivo transfection efficiency

2010 ◽  
Vol 144 (1) ◽  
pp. 46-54 ◽  
Author(s):  
Xin Zhao ◽  
Lichen Yin ◽  
Jieying Ding ◽  
Cui Tang ◽  
Shaohua Gu ◽  
...  
Keyword(s):  
Transfection Efficiency ◽  
Trimethyl Chitosan ◽  
Gene Carriers ◽  
In Vivo Transfection

Nanoincorporation of curcumin in polymer-glycerosomes and evaluation of their in vitro–in vivo suitability as pulmonary delivery systems

RSC Advances ◽  
2015 ◽  
Vol 5 (127) ◽  
pp. 105149-105159 ◽  
Author(s):  
Maria Letizia Manca ◽  
José E. Peris ◽  
Virginia Melis ◽  
Donatella Valenti ◽  
Maria Cristina Cardia ◽  
...  
Keyword(s):  
Sodium Hyaluronate ◽  
Pulmonary Delivery ◽  
Delivery Systems ◽  
Trimethyl Chitosan

This work was aimed at deliver curcumin to lungs by its incorporation into innovative vesicles glycerosomes and polymer-glycerosomes, the latter obtained combining glycerosomes with two polymers: sodium hyaluronate and trimethyl chitosan.

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