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Information Journal Paper

Title

Formulation and Evaluation of Nanocrystals of a Lipid Lowering Agent

Pages

  71-82

Abstract

Atorvastatin calcium, the lipid lowering agent, is taken as a model drug characterized by poor water solubility and Bioavailability. In this study an attempt was made for preparation of Nanocrystals using high pressure homogenization. A number of Stabilizers were included as well as polymers at different concentrations, and the formulations were homogenized for ten cycles at a pressure of 1000 bars. The obtained nano crystals were evaluated by determining their size, zeta potential, saturated solubility and dissolution rate. Results revealed that Formulation 3, containing (10: 1) drug to sodium lauryl sulphate ratio, possessed the highest saturated solubility and dissolution rate, and hence was analyzed by X-ray diffraction analysis, differential scanning calorimetry, Fourrier transform infrared spectroscopy and scanning electron microscopy. An in-vivo study was carried out on the successful formulation in comparison to drug powder using rats as experimental animals. A significant increase in the area under the concentration-time curve Cpmax and MRT for Nanocrystals was observed in comparison to the untreated Atorvastatin calcium.

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  • Cite

    APA: Copy

    Louis, Dina. (2016). Formulation and Evaluation of Nanocrystals of a Lipid Lowering Agent. IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR), 15(1), 71-82. SID. https://sid.ir/paper/288526/en

    Vancouver: Copy

    Louis Dina. Formulation and Evaluation of Nanocrystals of a Lipid Lowering Agent. IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR)[Internet]. 2016;15(1):71-82. Available from: https://sid.ir/paper/288526/en

    IEEE: Copy

    Dina Louis, “Formulation and Evaluation of Nanocrystals of a Lipid Lowering Agent,” IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH (IJPR), vol. 15, no. 1, pp. 71–82, 2016, [Online]. Available: https://sid.ir/paper/288526/en

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