Formulation and Evaluation of Galantamine Hydrobromide Proniosome Gel for Alzheimer’s disease

Authors

  • Mohammed Sarfaraz Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India
  • Tanvi Goel Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India
  • H. Doddayya Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

Abstract

Galantamine hydrobromide is formulated in tablets and capsules prescribed through oral delivery for the treatment of Alzheimer’s disease. However, oral delivery of drugs can cause severe side effects such as nausea, vomiting, and gastrointestinal disturbance. In the present research work, Galantamine hydrobromide is formulated as proniosome gel by Coacervation phase separation method using different surfactants such as Tweens and Spans. Overall eight formulations were developed and evaluated for various parameters. The prepared gels were viewed by naked eye to observe the colour of gel. Microscopical observations of the gels showed vesicles of optimum size from 3.030 mm (P2) - 3.735 mm (P5). The gel also showed optimum rate of spontaneity in the range 9.60 mm3x1000 (P7) to 11.80 mm3x1000 (P4) and entrapment efficiency of vesicles in the range 66.15% (P5) to 86.92% (P3). The gels had pH in suitable range of skin (5.92-6.9). The in vitro drug diffusion studies revealed that the drug diffusion was affected by the various surfactants used. The rank order of surfactant effect on in-vitro drug diffusion was Tween 80 > Tween 60 > Tween 40 >Tween 20 > Span 80 > Span 60 > Span 40 > Span 20. The proniosomal gel containing Tween 80 showed maximum drug diffusion (99.24%) and the gel containing Span 20 showed minimum drug diffusion (71.74%). FT-IR studies of optimized proniosome gel P8 revealed the absence of any chemical interactions between drug and carriers used.

Keywords: Galantamine hydrobromide, Proniosome gel, Coacervation phase separation method,   Surfactants, in vitro drug diffusion studies.

Keywords:

Galantamine hydrobromide, Proniosome gel, Coacervation phase separation method, Surfactants

DOI

https://doi.org/10.22270/jddt.v10i2-s.4027

Author Biographies

Mohammed Sarfaraz, Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

Tanvi Goel, Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

H. Doddayya, Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

Department of Pharmaceutics, NET Pharmacy College, Raichur- 584103, Karnataka, India

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Published

15-04-2020
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How to Cite

1.
Sarfaraz M, Goel T, Doddayya H. Formulation and Evaluation of Galantamine Hydrobromide Proniosome Gel for Alzheimer’s disease. J. Drug Delivery Ther. [Internet]. 2020 Apr. 15 [cited 2025 Feb. 14];10(2-s):68-74. Available from: https://jddtonline.info/index.php/jddt/article/view/4027

How to Cite

1.
Sarfaraz M, Goel T, Doddayya H. Formulation and Evaluation of Galantamine Hydrobromide Proniosome Gel for Alzheimer’s disease. J. Drug Delivery Ther. [Internet]. 2020 Apr. 15 [cited 2025 Feb. 14];10(2-s):68-74. Available from: https://jddtonline.info/index.php/jddt/article/view/4027