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Original Research

Fabrication and evaluation of valsartan–polymer– surfactant composite nanoparticles by using the supercritical antisolvent process

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Pages 5167-5176 | Published online: 07 Nov 2014

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Read on this site (9)

Yoon Tae Goo, Cheol-Ki Sa, Ji Yeh Choi, Min Song Kim, Chang Hyun Kim, Hyeon Kyun Kim & Young Wook Choi. (2021) Development of a Solid Supersaturable Micelle of Revaprazan for Improved Dissolution and Oral Bioavailability Using Box-Behnken Design. International Journal of Nanomedicine 16, pages 1245-1259.
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Shambhavi Borde, Sagar Kumar Paul & Harsh Chauhan. (2021) Ternary solid dispersions: classification and formulation considerations. Drug Development and Industrial Pharmacy 47:7, pages 1011-1028.
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Yoon Tae Goo, Seh Hyon Song, Dong Woo Yeom, Bo Ram Chae, Ho Yub Yoon, Chang Hyun Kim, Sun Young Park, Tae Hoon Kang, Sangkil Lee & Young Wook Choi. (2020) Enhanced oral bioavailability of valsartan in rats using a supersaturable self-microemulsifying drug delivery system with P-glycoprotein inhibitors. Pharmaceutical Development and Technology 25:2, pages 178-186.
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Dong Woo Yeom, Bo Ram Chae, Ho Yong Son, Jin Han Kim, Jun Soo Chae, Seh Hyon Song, Dongho Oh & Young Wook Choi. (2017) Enhanced oral bioavailability of valsartan using a polymer-based supersaturable self-microemulsifying drug delivery system. International Journal of Nanomedicine 12, pages 3533-3545.
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Sophia Yui Kau Fong, Annette Bauer-Brandl & Martin Brandl. (2017) Oral bioavailability enhancement through supersaturation: an update and meta-analysis. Expert Opinion on Drug Delivery 14:3, pages 403-426.
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Abdul Ahad, Mohd. Aqil, Kanchan Kohli, Yasmin Sultana & Mohd. Mujeeb. (2016) The ameliorated longevity and pharmacokinetics of valsartan released from a gel system of ultradeformable vesicles. Artificial Cells, Nanomedicine, and Biotechnology 44:6, pages 1457-1463.
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Eun-Sol Ha, Jeong-Soo Kim, In-hwan Baek, Jin-Wook Yoo, Yunjin Jung, Hyung Ryong Moon & Min-Soo Kim. (2015) Development of megestrol acetate solid dispersion nanoparticles for enhanced oral delivery by using a supercritical antisolvent process. Drug Design, Development and Therapy 9, pages 4269-4277.
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Eun-Sol Ha, In-hwan Baek, Jin-Wook Yoo, Yunjin Jung & Min-Soo Kim. (2015) Improving dissolution and oral bioavailability of pranlukast hemihydrate by particle surface modification with surfactants and homogenization. Drug Design, Development and Therapy 9, pages 3257-3266.
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Jae-Young Lee, Wie-Soo Kang, Jingpei Piao, In-Soo Yoon, Dae-Duk Kim & Hyun-Jong Cho. (2015) Soluplus®/TPGS-based solid dispersions prepared by hot-melt extrusion equipped with twin-screw systems for enhancing oral bioavailability of valsartan. Drug Design, Development and Therapy 9, pages 2745-2756.
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Rahul Kumar, Amit K. Thakur, Gergely Kali, Kancharlapalli Chinaraga Pitchaiah, Raj Kumar Arya & Anurag Kulabhi. (2022) Particle preparation of pharmaceutical compounds using supercritical antisolvent process: current status and future perspectives. Drug Delivery and Translational Research 13:4, pages 946-965.
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F. MUHANA, R. ABU-HUWAIJ, N. KHALAF, F. KHALILI & N. SHALAN. (2020) Synthesis and Characterization of Mesoporous Silica Carrier Releasing Valsartan. Asian Journal of Chemistry 32:11, pages 2927-2933.
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