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Optimization and characterization of deoxypodophyllotoxin loaded mPEG-PDLLA micelles by central composite design with response surface methodology.
Yu, Ying-Lan; Li, Ya-Nan; Zhang, Yong; Sun, Ru-Ning; Tu, Jia-Sheng; Shen, Yan.
Afiliação
  • Yu YL; Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
  • Li YN; Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
  • Zhang Y; Children's Hospital of Nanjing Medical University, Nanjing 210008, China.
  • Sun RN; Department of Professional Institute, China Pharmaceutical University, Nanjing 210009, China.
  • Tu JS; Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
  • Shen Y; Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China. Electronic address: shenyan19820801@126.com.
Chin J Nat Med ; 16(6): 471-480, 2018 Jun.
Article em En | MEDLINE | ID: mdl-30047469
ABSTRACT
The therapeutic application of deoxypodophyllotoxin (DPT) is limited due to its poor water solubility and stability. In the present study, the micelles assembled by the amphiphilic block copolymers (mPEG-PDLLA) were constructed to improve the solubility and safety of DPT for their in vitro and in vivo application. The central composite design was utilized to develop the optimal formulation composed of 1221.41 mg mPEG-PDLLA, the weight ratio of 1 4 (mPEG-PDLLA DPT), 30 mL hydration volume and the hydration temperature at 40 °C. The results showed that the micelles exhibited uniformly spherical shape with the diameter of 20 nm. The drug-loading and entrapment efficiency of deoxypodophyllotoxin-polymeric micelles (DPT-PM) were about (20 ± 2.84)% and (98 ± 0.79)%, respectively, indicating that the mathematical models predicted well for the results. Compared to the free DPT, the cytotoxicity showed that blank micelles possessed great safety for Hela cells. In addition, the DPT loaded micelle formulation achieved stronger cytotoxicity at the concentration of 1 × 10-7 mol·L-1, which showed significant difference from free DPT (P < 0.05). In conclusion, the micelles were highly promising nano-carriers for the anti-tumor therapy with DPT.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Podofilotoxina / Poliésteres / Polietilenoglicóis / Portadores de Fármacos / Desenho de Fármacos / Sistemas de Liberação de Medicamentos / Micelas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Podofilotoxina / Poliésteres / Polietilenoglicóis / Portadores de Fármacos / Desenho de Fármacos / Sistemas de Liberação de Medicamentos / Micelas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article