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| Preparation and in vitro transdermal study of paeoniflorin solid lipid nanoparticle gel |
| Hits 1008 Download times 516 Received:November 13, 2020 |
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| DOI
10.11656/j.issn.1672-1519.2021.03.24 |
| Key Words
paeoniflorin;solid lipid nanoparticle;gel;hot melt emulsification-homogenization method;Carbomer 940;transdermal absorption |
| Author Name | Affiliation | | XU Liqing | Department of Pharmacy, Dalian Third People's Hospital, Dalian 116033, China | | LIU Dan | Department of Pharmacy, Dalian Third People's Hospital, Dalian 116033, China | | TANG Wenjuan | Department of Pharmacy, Central Hospital of Shanghai Yangpu District, Shanghai 200090, China |
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| Abstract
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| [Objective] To prepare paeoniflorin solid lipid nanoparticle gel and evaluate its transdermal performance in vitro.[Methods] The paeoniflorin solid lipid nanoparticle were prepared by hot melt emulsification-homogenization method. The lipid-drug ratio (X1), solid lipid concentration (X2) and surfactant concentration (X3) were used as independent variables, with the average particle size (Y1) and the encapsulation efficiency (Y2) as dependent variables, the optimal formulation of paeoniflorin solid lipid nanoparticle was obtained by Box-Behnken experiment design. The microstructure of paeoniflorin solid lipid nanoparticle was observed by transmission electron microscope. The Carbomer 940 was used as a gel matrix to prepare paeoniflorin solid lipid nanoparticle gel. The in vitro transdermal absorption properties of Chonghe gel and paeoniflorin solid lipid nanoparticle gel were investigated by Franz diffusion cell method.[Results] The optimal formulation composition of paeoniflorin solid lipid nanoparticle as followed:the lipid-drug ratio was 80:1, the solid lipid concentration was 12.0 mg/mL, and the surfactant concentration was 10.0 mg/mL. The paeoniflorin solid lipid nanoparticle appeared to be spherical with uniform particle size distribution under the transmission electron microscope, the average particle size was (179.3±10.9) nm, and the encapsulation efficiency was (91.1±0.9)%. The drug accumulation transdermal amount of paeoniflorin solid lipid nanoparticle gels was significantly higher than that of Chonghe gel within 12 h, and the drug retention in skin was 4.8 times that of Chonghe gels.[Conclusion] The paeoniflorin solid lipid nanoparticle gel can significantly increase the cumulative transdermal delivery and increase the retention of drugs in the skin, and is expected to enhance the therapeutic effect of paeoniflorin on skin diseases. |
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