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Development of a fast dissolving film of epinephrine hydrochloride as a potential anaphylactic treatment for pediatrics.
Alayoubi, Alaadin; Haynes, Lindsay; Patil, Hemlata; Daihom, Baher; Helms, Richard; Almoazen, Hassan.
Affiliation
  • Alayoubi A; a Department of Pharmaceutical Sciences , University of Tennessee Health Science Center , Memphis , TN , USA.
  • Haynes L; b Department of Medicine , University of Tennessee Health Science Center , Memphis , TN , USA.
  • Patil H; c College of Pharmacy, University of Mississippi, University , MS , USA.
  • Daihom B; d Department of Pharmaceutics and Industrial Pharmacy , Cairo University, College of Pharmacy , Cairo , Egypt , and.
  • Helms R; e Department of Clinical Pharmacy , University of Tennessee Health Science Center , Memphis , TN , USA.
  • Almoazen H; a Department of Pharmaceutical Sciences , University of Tennessee Health Science Center , Memphis , TN , USA.
Pharm Dev Technol ; 22(8): 1012-1016, 2017 Dec.
Article in En | MEDLINE | ID: mdl-26740126
ABSTRACT

OBJECTIVE:

To develop a fast dissolving film strip containing epinephrine HCl for the potential treatment of pediatric anaphylaxis.

METHODS:

Four different films have been prepared by solvent casting technique where the percentages of the polymer (Lycoat RS720) were optimized. The polymer percentages were (20%, 25%, 27% and 30%) of the total formulation weighs. The thickness and elastic modulus of the optimized film was evaluated using dynamic mechanical analyzer. Epinephrine content uniformity was assessed using UV at wavelength 280 nm. For the dissolution test, fast dissolving films (FDFs) were evaluated in 500 Simulated Saliva, with 50 rpm. In vivo taste and disintegration evaluation was performed on six healthy volunteers.

RESULTS:

Films formed by formulations 1, 2 and 3 were too sticky after drying, while formulation 4 that has 30% polymer content formed smooth, transparent, flexible and uniform film, and therefore, it was selected for further testing. The value of elastic modulus was determined at 1.325 MPa. The thickness of the film at different locations was measured at 0.29 mm. Drug content in film was measured at 93% ±10. More than 90% of epinephrine was released from the film within 7.2 min. Bitterness of epinephrine was masked efficiently according to volunteer's comments with average disintegration time of 20 s.

CONCLUSION:

This study presents potential proof for using FDFs as a replacement therapy of epinephrine injections for pediatrics.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epinephrine Limits: Child / Humans Language: En Journal: Pharm Dev Technol Journal subject: FARMACIA Year: 2017 Document type: Article Affiliation country: United States Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epinephrine Limits: Child / Humans Language: En Journal: Pharm Dev Technol Journal subject: FARMACIA Year: 2017 Document type: Article Affiliation country: United States Publication country: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM