Fabrication, design, and in vivo investigation of mesoporous silica-based docetaxel trihydrate nanoparticles for colonic drug delivery

• Published in: Bulletin of the National Research Centre Vol. 47; no. 1; pp. 142 - 16
• Main Authors: Majumdar, Subhabrota, Mondal, Mohini, Bose, Anirbandeep, Kar, Ayan Kumar, Mazumder, Rana
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.12.2023; Springer Nature B.V; SpringerOpen
• Subjects: Agriculture; Bioavailability; Colorimetry; Controlled release; Docetaxel trihydrate; Drug delivery; Engineering; Evaluation parameters; Fabrication; Humanities and Social Sciences; In vivo methods and tests; In-vivo bioavailability study; Infrared spectroscopy; Lecithin; Mesoporous silica-based nanoparticles; multidisciplinary; Nanoparticles; Optimization; Oral administration; Pharmaceutical Industries; Phosphatidylcholine; Plasma levels; Polymers; Response surface methodology; Science; Science (multidisciplinary); Silica; Silicon dioxide; Tin; Zeta potential; Response surface methodology; Evaluation parameters; Docetaxel trihydrate; In-vivo bioavailability study; Mesoporous silica-based nanoparticles
• ISSN: 2522-8307; 2522-8307
• DOI: 10.1186/s42269-023-01117-7

Background Mesoporous silica-loaded docetaxel trihydrate nanoparticles are the potential to target drug delivery toward a specific region with high stability and predictable release at the target region. They have large surface areas and mesoporous structures with large pore volumes, leading to high bioavailability and therapeutic efficacy at the disease site. This study demonstrates how nanoparticles can be prepared using an emulsion technique. Results The ratios of eudragit S100 to eudragit L100 polymers, along with phosphatidylcholine, were varied according to the response surface methodology. Differential scanning colorimetry and fluorinated transmitted infrared spectroscopy studies showed that mesoporous silica particles were successful. All formulations had average particle sizes ranging from 70.65 to 143.01 nm, with a range of zeta potential from 17.6 ± 026 to 21 ± 011. In vitro drug delivery studies were achieved for all formulations with a zeta potential of 17.6 ± 026 to 21 ± 011. As per the statistical optimization by RSM that response model for percentage drug loading ( Y 1 ) was found to be 0.0002 which is p -value < 0.05. Hence, the model is significance. Accordingly percentage drug release at 6 h. ( Y 2 ) p -value was found to be 0.0001 and percentage drug release at 10 h ( Y 3 ) p -value was found to be 0.0002, respectively. So all the models are significant. After oral administration of the docetaxel, plasma levels were measured in vivo bioavailability testing of docetaxel. Docetaxel nanosuspension had a significantly higher C max amount than docetaxel microsuspension (98.03 ± 23.40 ng/ml and 213.67 ± 72.21 ng/ml, respectively, with t max 45 min). Docetaxel was more bioavailable in nanosuspension formulations, according to a bioavailability test of rats. Conclusion The results suggested that the mesoporous silica could be a great potential nanocarrier in colonic delivery with optimal drug content and controlled release docetaxel trihydrate.