Authors :
S. O. Abali; G. C. Onunkwo
Volume/Issue :
Volume 9 - 2024, Issue 4 - April
Google Scholar :
https://tinyurl.com/5n8fcfwn
Scribd :
https://tinyurl.com/ycxa34vh
DOI :
https://doi.org/10.38124/ijisrt/IJISRT24APR1028
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
The preparation and assessment of solid lipid
nanoparticles (SLNs) of nevirapine with improved oral
delivery for better management of HIV/AIDS was the aim
of this research. Eight batches of SLNs of nevirapine were
produced from Dika wax and evaluated for particle
charges and distribution of the sizes of particles using
Zeta sizer, surface shape with Cryo-Transmission
Electron Microspcope (Cryo-TEM), chemical interaction
between drug and excipients with Fourier Transform
Infrared Spectroscope (FTIR). Loading capacity,
encapsulation efficiency and in vitro drug release
properties were determined. Release profiles were
compared with ƒ2 statistic, one-way ANOVA and
students’t-test. From the results obtained, Cryo-TEM
revealed that the SLNs were round to oval in shape with
smooth external surface. Zeta sizer particle sizes and
distribution analysis indicated quality results for
Nevirapine SLN Batches 15 and 18. The zeta potential
results were: -16.83 ± 0.404 mV for Batch 1, -44.30 ±
0.624 mV for Batch 15 and -40.03 ± 2.65 mV for Batch 18.
Batches 15 and 18 SLNs had loading capacities of 6.71%
and 9.82% respectively and encapsulation efficiencies of
49.35% and 70.19% respectively. In vitro dissolution
showed 102% release for batch 18 and 87.5% release for
Batch 15 with a dissolution efficiency of 65% for Batch 15
and 83% for Batch 18 SLNs. ƒ2 statistic, ANOVA and
students’ t-test revealed Batch 15 SLNs are similar to
Batch 18 SLN. In conclusion, Batches 15 and 18 SLNs
have good properties for enhancing the delivery of
nevirapine as extended release dosage forms for better
management of HIV/AIDS.
Keywords :
Solid Lipid Nanoparticle, Nevirapine, Dika Wax, HIV/AIDS.
References :
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The preparation and assessment of solid lipid
nanoparticles (SLNs) of nevirapine with improved oral
delivery for better management of HIV/AIDS was the aim
of this research. Eight batches of SLNs of nevirapine were
produced from Dika wax and evaluated for particle
charges and distribution of the sizes of particles using
Zeta sizer, surface shape with Cryo-Transmission
Electron Microspcope (Cryo-TEM), chemical interaction
between drug and excipients with Fourier Transform
Infrared Spectroscope (FTIR). Loading capacity,
encapsulation efficiency and in vitro drug release
properties were determined. Release profiles were
compared with ƒ2 statistic, one-way ANOVA and
students’t-test. From the results obtained, Cryo-TEM
revealed that the SLNs were round to oval in shape with
smooth external surface. Zeta sizer particle sizes and
distribution analysis indicated quality results for
Nevirapine SLN Batches 15 and 18. The zeta potential
results were: -16.83 ± 0.404 mV for Batch 1, -44.30 ±
0.624 mV for Batch 15 and -40.03 ± 2.65 mV for Batch 18.
Batches 15 and 18 SLNs had loading capacities of 6.71%
and 9.82% respectively and encapsulation efficiencies of
49.35% and 70.19% respectively. In vitro dissolution
showed 102% release for batch 18 and 87.5% release for
Batch 15 with a dissolution efficiency of 65% for Batch 15
and 83% for Batch 18 SLNs. ƒ2 statistic, ANOVA and
students’ t-test revealed Batch 15 SLNs are similar to
Batch 18 SLN. In conclusion, Batches 15 and 18 SLNs
have good properties for enhancing the delivery of
nevirapine as extended release dosage forms for better
management of HIV/AIDS.
Keywords :
Solid Lipid Nanoparticle, Nevirapine, Dika Wax, HIV/AIDS.