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Nghiên cứu hệ vi tự nhũ chứa atorvastatin (2015)

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11. Dong Hoon Oha, Jun Hyeok Kanga, Dong Wuk Kim (2011), “Comparison of<br />

solid self-microemulsifying drug delivery system (solid SMEDDS) prepared with<br />

hydrophilic and hydrophobic solid carrier”, International Journal of Pharmaceutics,<br />

420, pp. 412.<br />

12. Durgacharan Arun Bhagwat, John Intru D’Souza (2012), “Formulation and<br />

evaluation of solid self micro emulsifying drug delivery system using aerosil 200 as<br />

solid carrier”, International Current Pharmaceutical Journal, 1 (12), pp. 414 – 419.<br />

13. Ganesh Shete, Vibha Puri, Lokesh Kumar, Ar<strong>vi</strong>nd K. Bansal (2010), “Solid<br />

State Characterization of Commercial Crystalline and Amorphous Atorvastatin<br />

Calcium Samples”, American Association of Pharmaceutical Scientists<br />

PharmSciTech, 2 (15), pp. 598.<br />

14. Goyal, Ankit Gupta (2012), “Self microemulsifying drug delivery system: a<br />

method for enhancement of bioavailability”, International journal of<br />

pharmaceutical sciences and research, 3 (1), pp. 66 – 79.<br />

15. HaiRong Shen, MingKang Zhong (2006), “Preparation and evaluation of selfmicroemulsifying<br />

drug delivery systems (SMEDDS) containing <strong>atorvastatin</strong>”,<br />

Journal of Pharmacy and Pharmacology, 58, pp. 1187.<br />

16. Hamed A. Chaus, Vitthal V. Chopade, Pra<strong>vi</strong>n D. Chaudhri (2013), "Self micron<br />

emulsifying drug delivery system: A re<strong>vi</strong>ew”, International Journal of<br />

Pharmaceutical sciences, 2 (1), pp. 34 – 44.<br />

17. Hanaa Mahmoud, Saleh Al-Suwayeh, Shaimaa Elkadi (2013), “Design and<br />

optimization of self-nanoemulsifying drug delivery systems of simvastatin aiming<br />

dissolution enhancement, African Journal of Pharmacy and Pharmacology, 7 (22),<br />

pp.1488 – 1489.<br />

18. Hira Choudhurya, Bapi Goraina, Sanmoy Karmakara, Easha Biswasa, Goutam<br />

Deyb, Rajib Barikc, Mahitosh Mandal, Tapan Kumar Pal (2013), “Improvement of<br />

cellular uptake, in <strong>vi</strong>tro antitumor acti<strong>vi</strong>ty and sustained release profile with<br />

DIỄN ĐÀN TOÁN - LÍ - HÓA 1000B TRẦN HƯNG ĐẠO TP.QUY NHƠN<br />

increased bioavailability from a nanoemulsion platform”, International Journal of<br />

Pharmaceutics, 460, pp. 131– 143.<br />

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