Nano lipidic carriers for codelivery of sorafenib and ganoderic acid for enhanced synergistic antitumor efficacy against hepatocellular carcinoma

The current study focuses on the development and evaluation of nano lipidic carriers (NLCs) for codelivery of sorafenib (SRF) and ganoderic acid (GA) therapy in order to treat hepatocellular carcinoma (HCC). The dual drug-loaded NLCs were prepared by hot microemulsion technique, where SRF and GA as...

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Veröffentlicht in:Saudi pharmaceutical journal 2021-08, Vol.29 (8), p.843-856
Hauptverfasser: Wang, Bin, Sun, Lin, Wen, Mingyun, Tan, Youchun, Almalki, Waleed H., Katouah, Hanadi, Kazmi, Imran, Afzal, Obaid, Altamimi, Abdulmalik Saleh Alfawaz, Al-Abbasi, Fahad A., Alrobaian, Majed, Alharbi, Khalid S., Alenezi, Sattam K., Alghaith, Adel F., Beg, Sarwar, Rahman, Mahfoozur
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Sprache:eng
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Zusammenfassung:The current study focuses on the development and evaluation of nano lipidic carriers (NLCs) for codelivery of sorafenib (SRF) and ganoderic acid (GA) therapy in order to treat hepatocellular carcinoma (HCC). The dual drug-loaded NLCs were prepared by hot microemulsion technique, where SRF and GA as the drugs, Precirol ATO5, Capmul PG8 as the lipids, while Solutol HS15 and ethanol was used as surfactant and cosolvents. The optimized drug-loaded NLCs were extensively characterized through in vitro and in vivo studies. The optimized formulation had particle size 29.28 nm, entrapment efficiency 93.1%, and loading capacity 14.21%. In vitro drug release studies revealed>64% of the drug was released in the first 6 h. The enzymatic stability analysis revealed stable nature of NLCs in various gastric pH, while accelerated stability analysis at 25◦C/60% RH indicated the insignificant effect of studied condition on particle size, entrapment efficiency, and loading capacity of NLCs. The cytotoxicity performed on HepG2 cells indicated higher cytotoxicity of SRF and GA-loaded NLCs as compared to the free drugs (p 
ISSN:1319-0164
2213-7475
DOI:10.1016/j.jsps.2021.06.006