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Published on:December 2019
Indian Journal of Pharmaceutical Education and Research, 2020; 54(1):xx-xx
Original Article | doi:10.5530/ijper.54.1.x

Intranasal Nalbuphine Formulation for Faster Management of Pain in Prehospital Scenario; Its Safety and Comparative Efficacy in Animal Models


Authors and affiliation (s):

Kushagra Khanna1, Deeksha Sharma1, Ritu Karwasra1, Nitin Sharma1, Dhruv Kumar Nishad1, Harvinder Popli2,*, Aseem Bhatnagar1

1Department of CEPIN, Institute of Nuclear Medicine and Allied Sciences (INMAS) Defence Research and Development Organization, Timarpur, Delhi, INDIA.

2Department of Pharmaceutics, Delhi Pharmaceutical Science and Research University, Delhi, Timarpur, INDIA.

Abstract:

Aim: Nalbuphine (NLB) is an approved opioid analgesic for the management of severe pain in wounds, battlefield injuries and is recommended to subsidize labour pain during childbirth. The study aims to develop an intranasal opioid formulation for faster pain relief. Secondly, to make feasible for the injured person or as buddy care compared to available parenteral formulations which require skilled persons for their administration. In case of war, accident or any natural calamities the feasibility of giving drugs from the parenteral route is not feasible as it requires high skilled medic/paramedic staff. Materials and Methods: Different formulations were made using NLB as an Active Pharmaceutical Ingredient (API), prepared formulations were characterized and evaluated for various parameters. The formulation F5 was optimized as it met the desired criteria. F5 was further studied for its efficacy in an established pain model using Eddy’s hot plate method and pain scoring in animals. Pharmacodynamics study was conducted in Sprague dawley rats which were further verified by gamma scintigraphy using 99mTc-pertechnetate labelled NLB showing significant and rapid deposition in the brain tissue. Results: NLB nasal formulation was optimized successfully; at pH 6.4±0.10 and viscosity 2.5±0.13 (cps). Osmolarity and percent drug release of optimized nasal drop at 240 min was found to be288±18 milliosmol/litre and 96.98±3.1% respectively. Gamma scintigraphy study results revealed that the formulation (F5) was able to deliver NLB to the brain within 10 mins of administration and remained localized up to 240 min. Pre-clinical subacute toxicity profiling of optimized formulation was done in Sprague dawley rats at 3X dose. Conclusion: Data obtained from the study indicate that the developed NLB nasal formulation has better efficacy for pain management than conventional I.M injection.

Key words: Nalbuphine, Nasal drop, Gamma scintigraphy, 99mTc-Pertechnetate, Subacute toxicity.

 

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IJPER - An Official Publication of Association of Pharmaceutical Teachers of India is pleased to announce continued growth in the 2019 Release of Journal Citation Reports (source: 2018 Web of Science Data).

 

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The Official Journal of Association of Pharmaceutical Teachers of India (APTI)
(Registered under Registration of Societies Act XXI of 1860 No. 122 of 1966-1967, Lucknow)

Indian Journal of Pharmaceutical Education and Research (IJPER) [ISSN-0019-5464] is the official journal of Association of Pharmaceutical Teachers of India (APTI) and is being published since 1967.

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