Authors :
Ritesh Fule; Prajakta Awachat
Volume/Issue :
Volume 11 - 2026, Issue 3 - March
Google Scholar :
https://tinyurl.com/2abavmc2
Scribd :
https://tinyurl.com/8bwe35bb
DOI :
https://doi.org/10.38124/ijisrt/26mar275
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
Nanostructured lipid carriers containing celecoxib were prepared to treat arthritis-associated Systemic Lupus
Erythematosus. CLX-NLC was formulated using hot emulsion ultrasonication method. In preparation of CLX-NLC, stearic
acid (solid lipid), oleic acid (liquid lipid), and tween 80 (surfactant) were used. A three-level three-factor box Behnken design
was adopted to optimize the formulated nano-structured lipid carrier system. The independent factors were solid lipid
amount (X1), liquid lipid amount (X2), and surfactant amount (X3). The examined responses were entrapment efficiency (Y1,
%), and particle size (Y2, nm). The optimum formula showed high entrapment efficiency of 81%, a small particle size of 138
nm, and a low polydispersity index of 0.248. FTIR spectroscopy shows that the celecoxib is compatible with other excipients
like stearic acid, oleic acid, and tween 80. In DSC the melting endothermic peak of celecoxib was not observed in the
thermogram of CLX-NLC showed the developed CLX-NLC formulation. The X-ray diffractogram of CLX-NLC showed
decrease in intensity of the peaks which leads to amorphization of drug. SEM micrographs revealed that the surface was
smooth of prepared NLC formulation and was in spherical shape nature. The in-vitro dissolution study showed a longer
retention time of 15 hours in CLX-NLC. In the storage stability study, optimized CLX-NLC was found to be stable for 3
months of storage in a room and accelerated stability conditions. In vivo pharmacokinetic research in Sprague- Dawley rats
displayed that the Cmax, Tmax, MRT, and AUC0-36 hrs were increased two times as compared to pure drug. Current study
confirms that CLX-NLC will be an effective medication therapy for SLE patients.
Keywords :
Systemic Lupus Erythematosus, Celecoxib, Nano Lipid Carrier System, Sustained Release.
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Nanostructured lipid carriers containing celecoxib were prepared to treat arthritis-associated Systemic Lupus
Erythematosus. CLX-NLC was formulated using hot emulsion ultrasonication method. In preparation of CLX-NLC, stearic
acid (solid lipid), oleic acid (liquid lipid), and tween 80 (surfactant) were used. A three-level three-factor box Behnken design
was adopted to optimize the formulated nano-structured lipid carrier system. The independent factors were solid lipid
amount (X1), liquid lipid amount (X2), and surfactant amount (X3). The examined responses were entrapment efficiency (Y1,
%), and particle size (Y2, nm). The optimum formula showed high entrapment efficiency of 81%, a small particle size of 138
nm, and a low polydispersity index of 0.248. FTIR spectroscopy shows that the celecoxib is compatible with other excipients
like stearic acid, oleic acid, and tween 80. In DSC the melting endothermic peak of celecoxib was not observed in the
thermogram of CLX-NLC showed the developed CLX-NLC formulation. The X-ray diffractogram of CLX-NLC showed
decrease in intensity of the peaks which leads to amorphization of drug. SEM micrographs revealed that the surface was
smooth of prepared NLC formulation and was in spherical shape nature. The in-vitro dissolution study showed a longer
retention time of 15 hours in CLX-NLC. In the storage stability study, optimized CLX-NLC was found to be stable for 3
months of storage in a room and accelerated stability conditions. In vivo pharmacokinetic research in Sprague- Dawley rats
displayed that the Cmax, Tmax, MRT, and AUC0-36 hrs were increased two times as compared to pure drug. Current study
confirms that CLX-NLC will be an effective medication therapy for SLE patients.
Keywords :
Systemic Lupus Erythematosus, Celecoxib, Nano Lipid Carrier System, Sustained Release.