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Production and characterization of testosterone undecanoate-loaded NLC for oral bioavailability enhancement
被引:38
|作者:
Muchow, M.
[1
,2
]
Maincent, P.
[2
]
Mueller, R. H.
[1
]
Keck, C. M.
[1
,3
]
机构:
[1] Free Univ Berlin, Dept Pharmaceut Biopharmaceut & NutriCosmet, D-12169 Berlin, Germany
[2] Univ Nancy 1, Lab Pharmaceut Technol & Biopharm, Nancy, France
[3] Univ Putra Malaysia, Lab Mol Biomed, Inst Biosci, Serdaug, Malaysia
关键词:
DSC;
lipid nanoparticles;
NLC;
oral bioavailability;
testosterone undecanoate;
LIPID NANOPARTICLES SLN;
PARTICLE-SIZE REDUCTION;
DRUG-DELIVERY;
LIPOPHILIC DRUGS;
FORMULATIONS;
SURFACTANTS;
SUSPENSIONS;
DEGRADATION;
TECHNOLOGY;
TRANSPORT;
D O I:
10.3109/03639045.2010.489559
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Purpose: Nanostructured lipid carriers were loaded with testosterone undecanoate (TU), which has a low oral bioavailability. Methods: Different NLC dispersions were produced using the hot high pressure homogenization method. Particles were characterized using dynamic and static light scattering techniques, differential scanning calorimetry and X-ray diffraction. And the bioavailability was compared to a marketed product. Results: Nanostructured lipid carriers with up to 30% TU load and sizes of about 600 and 200 nm could be achieved, allowing a direct comparison of the size effect in in vivo bioavailability studies. The zeta potentials varied between -20 and -40 mV. The bioavailability of Andriol Testocaps (R) in the fed state was matched. Conclusions: This opens the perspective of administering a single dose of dose of TU in one oral dosage unit and simultaneously having a bioavailability less dependent on the fed state.
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页码:8 / 14
页数:7
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