Development of a Sustained Release Solid Dispersion Using Swellable Polymer by Melting Method
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Tuong Ngoc-Gia Nguyen
[1
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Phuong Ha-Lien Tran
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Vietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
Deakin Univ, Sch Med, Waurn Ponds, Vic, AustraliaVietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
Phuong Ha-Lien Tran
[1
,2
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Toi Van Vo
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Vietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, VietnamVietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
Toi Van Vo
[1
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Duan, Wei
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Deakin Univ, Sch Med, Waurn Ponds, Vic, AustraliaVietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
Duan, Wei
[2
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Thao Truong-Dinh Tran
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Vietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
Deakin Univ, Inst Frontier Mat, Waurn Ponds, Vic, AustraliaVietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
Thao Truong-Dinh Tran
[1
,3
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[1] Vietnam Natl Univ, Int Univ, Dept Biomed Engn, Pharmaceut Engn Lab, Ho Chi Minh City, Vietnam
[2] Deakin Univ, Sch Med, Waurn Ponds, Vic, Australia
[3] Deakin Univ, Inst Frontier Mat, Waurn Ponds, Vic, Australia
This study is to design a sustained release solid dispersion using swellable polymer by melting method. Polyethylene glycol 6000 (PEG 6000) and hydroxypropyl methylcellulose 4000 (HPMC 4000) were used in solid dispersion for not only enhancing drug dissolution rate but also sustaining drug release. HPMC 4000 is a common swellable polymer in matrix sustained release dosage form, but could not be used in preparation of solid dispersion by melting method. However, the current study utilized the swelling capability of HPMC 4000 accompanied by the common carrier PEG 6000 in solid dispersion to accomplish the goal. While PEG 6000 acted as a releasing stimulant carrier and provided an environment to facilitate the swelling of HPMC 4000, this swellable polymer could act as a rate-controlling agent. This greatly assisted the dissolution enhancement by changing the crystalline structure of drug to more amorphous form and creating a molecular interaction. These results suggested that this useful technique can be applied in designing a sustained release solid dispersion with many advantages.