Izvorni znanstveni članak

https://doi.org/10.1515/acph-2017-0034

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

MUHAMMAD HANIF ; Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan
HAFEEZ ULLAH KHAN ; Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan; Faculty of Pharmacy, University of Sargodha, Sargodha, Pakistan
SAMINA AFZAL ; Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan
ASIF MAHMOOD ; Instituteof Pharmacy, Physiology and Pharmacology, University of Agriculture Faisalabad
SAFIRAH MAHEEN ; Faculty of Pharmacy, Bahauddin Zakariya University, Multan, Pakistan
KHURRAM AFZAL ; Department of Food sciences, Bahauddin Zakariya University, Multan, Pakistan
NABILA IQBAL ; Faculty of Pharmacy, University of Sargodha, Sargodha, Pakistan
MEHWISH ANDLEEB ; Faculty of Pharmacy and Alternative Medicines, Islamia University, Bahawalpur, Pakistan
NAZAR ABBAS ; Ranesearch and Development, Mass Pharma(Pvt) Ltd, Lahore, Pakistan; Rashid Latif College of Pharmacy, Lahore, Pakistan

Sažetak

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 (Y1), entrapment efficiency (Y2) and drug release (Y3). SLMs having a 10–40 µm 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 Y1 (29–86 %), Y2 (45–83 %) and Y3 (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.

Ključne riječi

central composite design; differential scanning calorimetry; solid lipid microparticles; microencapsulation; nebivolol; carnauba wax

Hrčak ID:

186322

URI

https://hrcak.srce.hr/186322

Datum izdavanja:

31.12.2017.

Posjeta: 997 *