مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

413
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

183
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

PREPARATION, CHARACTERIZATION AND OPTIMIZATION OF SILDENAFIL CITRATE LOADED PLGA NANOPARTICLES BY STATISTICAL FACTORIAL DESIGN

Pages

  1-10

Abstract

 Background and the aim of the study: The objective of the present study was to formulate and optimize NANOPARTICLEs (NPs) of sildenafil-loaded poly (lactic-co-glycolic acid) (PLGA) by DOUBLE EMULSION solvent evaporation (DESE) method. The relationship between design factors and experimental data was evaluated using response surface methodology.Method: A BOX-BEHNKEN design was made considering the mass ratio of drug to polymer (D/P), the volumetric proportion of the water to oil phase (W/O) and the concentration of polyvinyl alcohol (PVA) as the independent agents. PLGA-NPs were successfully prepared and the size (nm), entrapment efficiency (EE), drug loading (DL) and cumulative release of drug from NPs post 1 and 8 hrs were assessed as the responses.Results: The NPs were prepared in a spherical shape and the sizes range of 240 to 316 nm. The polydispersity index of size was lower than 0.5 and the EE (%) and DL (%) varied between 14-62% and 2-6%, respectively. The optimized formulation with a desirability factor of 0.9 was selected and characterized. This formulation demonstrated the particle size of 270 nm, EE of 55%, DL of 3.9% and cumulative drug release of 79% after 12 hrs. In vitro release studies showed a burst release at the initial stage followed by a sustained release of sildenafil from NPs up to 12 hrs.The release kinetic of the optimized formulation was fitted to Higuchi model.Conclusions: SILDENAFIL CITRATE NPs with small particle size, lipophilic feature, high entrapment efficiency and good loading capacity is produced by this method. Characterization of optimum formulation, provided by an evaluation of experimental data, showed no significant difference between calculated and measured data.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    GHASEMIAN, ELHAM, VATANARA, ALIREZA, ROUHOLAMINI NAJAFABADI, ABDOLHOSSEIN, ROUINI, MOHAMMAD REZA, GILANI, KAMBIZ, & DARABI, MAJID. (2013). PREPARATION, CHARACTERIZATION AND OPTIMIZATION OF SILDENAFIL CITRATE LOADED PLGA NANOPARTICLES BY STATISTICAL FACTORIAL DESIGN. DARU JOURNAL OF PHARMACEUTICAL SCIENCE, 21(9), 1-10. SID. https://sid.ir/paper/275744/en

    Vancouver: Copy

    GHASEMIAN ELHAM, VATANARA ALIREZA, ROUHOLAMINI NAJAFABADI ABDOLHOSSEIN, ROUINI MOHAMMAD REZA, GILANI KAMBIZ, DARABI MAJID. PREPARATION, CHARACTERIZATION AND OPTIMIZATION OF SILDENAFIL CITRATE LOADED PLGA NANOPARTICLES BY STATISTICAL FACTORIAL DESIGN. DARU JOURNAL OF PHARMACEUTICAL SCIENCE[Internet]. 2013;21(9):1-10. Available from: https://sid.ir/paper/275744/en

    IEEE: Copy

    ELHAM GHASEMIAN, ALIREZA VATANARA, ABDOLHOSSEIN ROUHOLAMINI NAJAFABADI, MOHAMMAD REZA ROUINI, KAMBIZ GILANI, and MAJID DARABI, “PREPARATION, CHARACTERIZATION AND OPTIMIZATION OF SILDENAFIL CITRATE LOADED PLGA NANOPARTICLES BY STATISTICAL FACTORIAL DESIGN,” DARU JOURNAL OF PHARMACEUTICAL SCIENCE, vol. 21, no. 9, pp. 1–10, 2013, [Online]. Available: https://sid.ir/paper/275744/en

    Related Journal Papers

  • No record.
  • Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button