Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology

被引:4
|
作者
Hanif, Muhammad [1 ]
Khan, Hafeez Ullah [1 ,2 ]
Afzal, Samina [1 ]
Mahmood, Asif [3 ]
Maheen, Safirah [2 ]
Afzal, Khurram [4 ]
Iqbal, Nabila [2 ]
Andleeb, Mehwish [5 ]
Abbas, Nazar [6 ,7 ]
机构
[1] Bahauddin Zakariya Univ, Fac Pharm, Multan, Pakistan
[2] Univ Sargodha, Fac Pharm, Sargodha, Pakistan
[3] Univ Agr Faisalabad, Inst Pharm Physiol & Pharmacol, Faisalabad, Pakistan
[4] Bahauddin Zakariya Univ, Dept Food Sci, Multan, Pakistan
[5] Islamia Univ Bahawalpur, Fac Pharm & Alternat Med, Bahawalpur, Pakistan
[6] Res & Dev Mass Pharma Pvt Ltd, Lahore, Pakistan
[7] Rashid Latif Coll Pharm, Lahore, Pakistan
关键词
central composite design; differential scanning calorimetry; solid lipid microparticles; microencapsulation; nebivolol; carnauba wax; IN-VITRO EVALUATION; DRUG-DELIVERY; WAX MICROPARTICLES; NANOPARTICLES; MICROSPHERES; CARVEDILOL; DESIGN; VARIABLES; EXCIPIENT; SYSTEM;
D O I
10.1515/acph-2017-0034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
For preparing nebivolol loaded solid lipid microparticles (SLMs) by the solvent evaporation microencapsulation process from carnauba wax and glyceryl monostearate, central composite design was used to study the impact of independent variables on yield (Y-1), entrapment efficiency (Y-2) and drug release (Y-3). SLMs having a 10-40 mu m size range, with good rheological behavior and spherical smooth surfaces, were produced. Fourier transform infrared spectroscopy, differential scanning calorimetry and X-ray diffractometry pointed to compatibility between formulation components and the zeta-potential study confirmed better stability due to the presence of negative charge (-20 to -40 mV). The obtained outcomes for Y-1 (29-86 %), Y-2 (45-83 %) and Y-3 (49-86 %) were analyzed by polynomial equations and the suggested quadratic model were validated. Nebivolol release from SLMs at pH 1.2 and 6.8 was significantly (p < 0.05) affected by lipid concentration. The release mechanism followed Higuchi and zero order models, while n > 0.85 value (Korsmeyer-Peppas) suggested slow erosion along with diffusion. The optimized SLMs have the potential to improve nebivolol oral bioavailability.
引用
收藏
页码:441 / 461
页数:21
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