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Intranasal delivery of asenapine loaded nanostructured lipid carriers : formulation, characterization, pharmacokinetic and behavioural assessment

Singh, Sanjay Kumar (författare)
Department of Pharmaceutics, Indian Institute of Technology, Banaras Hindu University, Varanas
Dadhania, Parth (författare)
Pharma Research, Lupin Limited (Research Park), Pune
Vuddanda, Parameswara Rao (författare)
Luleå tekniska universitet,Medicinsk vetenskap
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Jain, Achint K. (författare)
Department of Pharmaceutics, Indian Institute of Technology, Banaras Hindu University, Varanas
Velaga, Sitaram (författare)
Luleå tekniska universitet,Medicinsk vetenskap
Singh, Sanjay (författare)
Department of Pharmaceutics, Indian Institute of Technology, Banaras Hindu University, Varanas
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 (creator_code:org_t)
2016
2016
Engelska.
Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 6:3, s. 2032-2045
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • The aim of the present research work was to develop asenapine (ASM) loaded nanostructured lipid carriers (ANLC) for the delivery of drugs in the brain by an intranasal route to enhance therapeutic efficacy. A quality by design approach was used for development and optimization of ANLC. A total of five independent variables were selected, in which three were compositions and two were process variables, while particle size and entrapment efficiency were selected as response variables. The final optimized batch was evaluated by various in vitro characterizations as well as in vivo brain and plasma pharmacokinetic studies. Finally, the ANLC was assessed for efficacy and safety profiling for upto three weeks by a behavior model viz. catalepsy, induced locomotor and paw test in Charles Foster rats. The observed particle size, entrapment efficiency and zeta potential of ANLC was found to be 167.30 +/- 7.52 nm, 83.50 +/- 2.48% and -4.33 +/- 1.27 mV, respectively. Surface characterization studies demonstrated a spherical shape with a smooth surface of ANLC which follows the Korsmeyer-Peppas in vitro release kinetic model (r(2) = 0.9911, n = 0.53). A brain pharmacokinetic study indicated a significantly higher (p < 0.05) peak drug concentration (C-max: 74.13 +/- 6.73 ng mL(-1)), area under the drug concentration-time curve (AUC(0-24) (h): 560.93 +/- 27.85 h ng mL(-1)) and mean residence time (MRT: 7.1 +/- 0.13 h) of ANLC compared to ASM in the brain via an intranasal route. The results of behaviour studies of ANLC showed a significant decrease in extra-pyramidal side effects with increasing antipsychotic effect after 1-2 week(s) of treatment. These findings demonstrate that nanostructured lipid carriers could be a new promising drug delivery system for intranasal delivery of asenapine in the treatment of schizophrenia

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Annan hälsovetenskap (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Other Health Sciences (hsv//eng)

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Health Science
Hälsovetenskap

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