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DDC
| 615 | |
Tác giả CN
| Dương, Thị Hồng Ánh | |
Nhan đề
| Nghiên cứu bào chế hệ nano chất mang lipid chứa curcumin / Dương Thị Hồng Ánh, Phạm Thị Hằng | |
Tóm tắt
| As curcumin (a polyphenol in nature, isolated from tumeric Curcuma longa L.) is well-known for its antioxidant and ant-inflammatory activity; yet, its use is more or less limited due to its poor oral bioavailability resuting from its poor water solubilty, poor oral absorption, extensive metabolism in the liver and rapid elimination from the body; to overcome these all, a curcumin-nanostructured lipid carrier system was formulated for oral delivery. Influences of solid lipid (glycerin monostearat and cetylic alcol), liquid lipid (Labrafac PG, Labrafac lipophile and Miglyol® 812), surfactants (Tween 80 and Span 80) and preparation operation on the mean particle size, polydispersity index and in vitro drug release were studied. The obtained curcumin-nanostructured lipid carrier system with glycerin monostearate, Labrafac lipophile, Span 80 and Tween 80 achieved desirably small mean particle size (147.3 ± 16.4 nm) along with polydispersity index (0.404 ± 0.017) and drug release of 40.3% after 8 hrs.
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Thuật ngữ chủ đề
| Nghiên cứu - Kỹ thuật --Việt Nam | |
Từ khóa tự do
| Curcumin | |
Từ khóa tự do
| Lipid | |
Từ khóa tự do
| Nano | |
Tác giả(bs) CN
| Phạm, Thị Hằng | |
Nguồn trích
| Tạp chí Dược học 2018tr. 59-63
Số: 02 |
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000
| 00000nab#a2200000ui#4500 |
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| 001 | 18894 |
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| 002 | 9 |
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| 004 | 557034D8-EE43-4549-9433-09450E8BC2AD |
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| 005 | 201912131108 |
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| 008 | 081223s vm| vie |
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| 009 | 1 0 |
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| 039 | |y20191213110804|zthienvan |
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| 082 | |a615 |
|---|
| 100 | |aDương, Thị Hồng Ánh |
|---|
| 245 | |aNghiên cứu bào chế hệ nano chất mang lipid chứa curcumin / |cDương Thị Hồng Ánh, Phạm Thị Hằng |
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| 520 | |aAs curcumin (a polyphenol in nature, isolated from tumeric Curcuma longa L.) is well-known for its antioxidant and ant-inflammatory activity; yet, its use is more or less limited due to its poor oral bioavailability resuting from its poor water solubilty, poor oral absorption, extensive metabolism in the liver and rapid elimination from the body; to overcome these all, a curcumin-nanostructured lipid carrier system was formulated for oral delivery. Influences of solid lipid (glycerin monostearat and cetylic alcol), liquid lipid (Labrafac PG, Labrafac lipophile and Miglyol® 812), surfactants (Tween 80 and Span 80) and preparation operation on the mean particle size, polydispersity index and in vitro drug release were studied. The obtained curcumin-nanostructured lipid carrier system with glycerin monostearate, Labrafac lipophile, Span 80 and Tween 80 achieved desirably small mean particle size (147.3 ± 16.4 nm) along with polydispersity index (0.404 ± 0.017) and drug release of 40.3% after 8 hrs.
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| 650 | |aNghiên cứu - Kỹ thuật |zViệt Nam |
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| 653 | |aCurcumin |
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| 653 | |aLipid |
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| 653 | |aNano |
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| 700 | |aPhạm, Thị Hằng |
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| 773 | |tTạp chí Dược học |d2018|gtr. 59-63|i02 |
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| 890 | |c1|a0|b0|d3 |
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