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

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 releas...

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Main Authors: Hanif Muhammad, Khan Hafeez Ullah, Afzal Samina, Mahmood Asif, Maheen Safirah, Afzal Khurram, Iqbal Nabila, Andleeb Mehwish, Abbas Nazar
Format: Article
Language:English
Published: Sciendo 2017-12-01
Series:Acta Pharmaceutica
Subjects:
Online Access:https://doi.org/10.1515/acph-2017-0034
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spelling doaj-562e00bf322e49f59d7a829aab9dd3562021-09-06T19:39:39ZengSciendoActa Pharmaceutica1846-95582017-12-0167444146110.1515/acph-2017-0034acph-2017-0034Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodologyHanif Muhammad0Khan Hafeez Ullah1Afzal Samina2Mahmood Asif3Maheen Safirah4Afzal Khurram5Iqbal Nabila6Andleeb Mehwish7Abbas Nazar8Faculty of Pharmacy, Bahauddin Zakariya University, Multan, PakistanFaculty of Pharmacy, Bahauddin Zakariya University, Multan, PakistanFaculty of Pharmacy, Bahauddin Zakariya University, Multan, PakistanFaculty of Pharmacy, Bahauddin Zakariya University, Multan, PakistanFaculty of Pharmacy, University of Sargodha, Sargodha, PakistanDepartment of Food sciences Bahauddin Zakariya University Multan, PakistanFaculty of Pharmacy, University of Sargodha, Sargodha, PakistanFaculty of Pharmacy and Alternative Medicines, Islamia University Bahawalpur, PakistanResearch and Development Mass Pharma(Pvt) Ltd, Lahore, PakistanFor 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.https://doi.org/10.1515/acph-2017-0034central composite designdifferential scanning calorimetrysolid lipid microparticlesmicroencapsulationnebivololcarnauba wax
collection DOAJ
language English
format Article
sources DOAJ
author Hanif Muhammad
Khan Hafeez Ullah
Afzal Samina
Mahmood Asif
Maheen Safirah
Afzal Khurram
Iqbal Nabila
Andleeb Mehwish
Abbas Nazar
spellingShingle Hanif Muhammad
Khan Hafeez Ullah
Afzal Samina
Mahmood Asif
Maheen Safirah
Afzal Khurram
Iqbal Nabila
Andleeb Mehwish
Abbas Nazar
Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology
Acta Pharmaceutica
central composite design
differential scanning calorimetry
solid lipid microparticles
microencapsulation
nebivolol
carnauba wax
author_facet Hanif Muhammad
Khan Hafeez Ullah
Afzal Samina
Mahmood Asif
Maheen Safirah
Afzal Khurram
Iqbal Nabila
Andleeb Mehwish
Abbas Nazar
author_sort Hanif Muhammad
title Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology
title_short Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology
title_full Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology
title_fullStr Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology
title_full_unstemmed Sustained release biodegradable solid lipid microparticles: Formulation, evaluation and statistical optimization by response surface methodology
title_sort sustained release biodegradable solid lipid microparticles: formulation, evaluation and statistical optimization by response surface methodology
publisher Sciendo
series Acta Pharmaceutica
issn 1846-9558
publishDate 2017-12-01
description 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.
topic central composite design
differential scanning calorimetry
solid lipid microparticles
microencapsulation
nebivolol
carnauba wax
url https://doi.org/10.1515/acph-2017-0034
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