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Formulation of Fast Dissolving Tablets of Lisinopril Using Combination of Synthetic Superdisintegrants


Affiliations
1 Royal College of Pharmacy and Health Sciences - Berhampur, India
2 St. Ann's college of Pharmacy, Cantonment- Vizianagram, India
3 Berhampur University- Berhampur, India
4 Himalayan Institute of Pharmacy, Sikkim, India
     

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Fast dissolving tablets of Lisinopril were designed using combination of synthetic superdisintegrants like croscarmellose sodium, crospovidone and sodium starch glycolate in a ratio of 5:10 and 10:5 respectively by direct compression method. The blends of all formulations were evaluated for various pre-formulation factors. Tablets were evaluated for weight variation, hardness, disintegration time, drug content, friability and in vitro dissolution. The formulation of Lisinopril containing 10% crospovidone and 5% croscarmellose showed disintegration time of 145±0.502 secs respectively with 99% drug release within 30 mins. The results showed that super disintegrants used in combinations shows better disintegrating property. The FTIR spectra showed no interactions among them.

Keywords

Fast Dissolving Tablet, Lisinopril, Croscarmellose Sodium, Crospovidone, Sodium Starch Glycolate.
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  • Formulation of Fast Dissolving Tablets of Lisinopril Using Combination of Synthetic Superdisintegrants

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Authors

Rajeshree Panigrahi
Royal College of Pharmacy and Health Sciences - Berhampur, India
K. A. Chowdary
St. Ann's college of Pharmacy, Cantonment- Vizianagram, India
Gitanjali Mishra
Berhampur University- Berhampur, India
Manas Bhowmik
Himalayan Institute of Pharmacy, Sikkim, India
Saiprasanna Behera
Royal College of Pharmacy and Health Sciences - Berhampur, India

Abstract


Fast dissolving tablets of Lisinopril were designed using combination of synthetic superdisintegrants like croscarmellose sodium, crospovidone and sodium starch glycolate in a ratio of 5:10 and 10:5 respectively by direct compression method. The blends of all formulations were evaluated for various pre-formulation factors. Tablets were evaluated for weight variation, hardness, disintegration time, drug content, friability and in vitro dissolution. The formulation of Lisinopril containing 10% crospovidone and 5% croscarmellose showed disintegration time of 145±0.502 secs respectively with 99% drug release within 30 mins. The results showed that super disintegrants used in combinations shows better disintegrating property. The FTIR spectra showed no interactions among them.

Keywords


Fast Dissolving Tablet, Lisinopril, Croscarmellose Sodium, Crospovidone, Sodium Starch Glycolate.