Author(s): Arifa Begum Sk, Padma Sree V, Anusha V, Keerthi Veronica Z, Vinitha Sree P, Prameela K, Nazeema MD, Padmalatha K

Email(s): arifashaik2007@gmail.com

DOI: 10.5958/0974-360X.2018.00899.5   

Address: Arifa Begum Sk*1, Padma Sree V2, Anusha V2, Keerthi Veronica Z2, Vinitha Sree P2, Prameela K2, Nazeema MD2, Padmalatha K2
1Chalapathi Institute of Pharmaceutical Sciences, Chalapathi Nagar, Lam, Guntur – 522034, Andhra Pradesh, India.
2Vijaya Institute of Pharmaceutical Sciences for Women, Enikepadu, Vijayawada – 521108, Andhra Pradesh, India.
*Corresponding Author

Published In:   Volume - 11,      Issue - 11,     Year - 2018


ABSTRACT:
Medicated oral jelly formulations are more preferable for pediatric patients, which provide rapid dissolution and absorption of drugs thereby early onset of action. The aim of the present investigation was to formulate and evaluate oral jelly formulations of salbutamol sulphate. Salbutamol sulphate oral jellies were prepared using gelatin alone, methyl cellulose-gelatin and sodium carboxy methyl cellulose-gelatin in combination as gelling agents. The prepared jelly formulations were evaluated for pre-formulation studies, physical characteristics, drug content, pH, rheological properties, syneresis and in vitro dissolution testing. Fourier transform infrared analysis showed that there was no incompatibility between drug and excipients. The pH of all the formulations was found between pH 6.54 ± 0.06 and 6.74 ± 0.02. The weight variation was found between 0.99% ± 1.24 and 1.01% ± 0.74 in all prepared jelly formulations. The drug content was found in the range of 98.23% ± 0.58 to 99.25% ± 0.35, which was in conformity with the pharmacopoeial specification of 98% - 101%. Syneresis was not observed in jellies. All formulations showed more than 50% drug release within 15 min. From the results of in vitro dissolution study, it was found that the rate of dissolution of salbutamol sulphate from F5 (gelatin - methyl cellulose combination) and F7 (gelatin - sodium CMC combination) was found to be higher and in conformance with the bio-pharmaceutical classification system (BCS) concept for the immediate release formulations (>85% in 30 min).


Cite this article:
Arifa Begum Sk, Padma Sree V, Anusha V, Keerthi Veronica Z, Vinitha Sree P, Prameela K, Nazeema MD, Padmalatha K. Formulation and Evaluation of Pediatric Oral Soft Jellies of Salbutamol Sulphate. Research J. Pharm. and Tech 2018; 11(11): 4939-4945. doi: 10.5958/0974-360X.2018.00899.5

Cite(Electronic):
Arifa Begum Sk, Padma Sree V, Anusha V, Keerthi Veronica Z, Vinitha Sree P, Prameela K, Nazeema MD, Padmalatha K. Formulation and Evaluation of Pediatric Oral Soft Jellies of Salbutamol Sulphate. Research J. Pharm. and Tech 2018; 11(11): 4939-4945. doi: 10.5958/0974-360X.2018.00899.5   Available on: https://rjptonline.org/AbstractView.aspx?PID=2018-11-11-31


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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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