Original ArticleIndian Journal of Pharmaceutical Education and ResearchVol. 60 | Issue 3 | 2026 | pp. 1061–1069Open access
Optimized Formulation of Carvedilol Fast-Dissolving Tablets Using Modified Super disintegrants: Breaking Solubility Barriers of BCS Class II Drugs
- 1,2,
- 1*
- 1 Department of Pharmaceutics, GITAM School of Pharmacy, GITAM (Deemed to be University), Rushikonda, Visakhapatnam, Andhra Pradesh, INDIA.
- 2 Department of Pharmaceuitcs, School of Pharmacy, Godavari Global University, Rajahmundry, East Godavari, Andhra Pradesh, INDIA.
Published in Indian Journal of Pharmaceutical Education and Research
Correspondence: Santosh Kumar Rada
Department of Pharmaceutics, GITAM School of Pharmacy, GITAM (Deemed to be University), Rushikonda, Visakhapatnam, Andhra Pradesh, INDIA.
Email: anilvadaga@gmail.com
Copyright: © 2026 Manuscript Technomedia. This is an open access article.
- Published:
- Apr 23, 2026
- Received:
- Jan 27, 2026
- Accepted:
- Apr 18, 2026
How to cite
Vadaga, A., & Rada, S. K. (2026). Optimized Formulation of Carvedilol Fast-Dissolving Tablets Using Modified Super disintegrants: Breaking Solubility Barriers of BCS Class II Drugs. Indian Journal of Pharmaceutical Education and Research, 60(3), 1061–1069. https://doi.org/10.5530/ijper.20261525
Abstract
Background: The BCS Class-II faces major challenge, low solubility and poor bioavailability issues. Carvedilol, an anti-hypertensive drugs, has a bioavailability 20-25%. Objectives: This research focuses on the development of fast dissolving tablets for Carvedilol (CARV), utilizing sorghum starch modified with humic acid as a novel superdisintegrant through factorial design to achieve rapid drug dissolution, bioavailability and patient compliance. Materials and Methods: Sorghum starch was isolated through a modified alkaline treating method from sorghum flour then it was modified with humic acid to form starch humate. Various tests such as gelatinization, viscosity, pH and flowability were performed. Quality by design was applied to identify the most important characteristics (response variables) such as disintegration time, dissolution efficiency and cumulative percent drug dissolved at the end of 10 min. The independent variables are starch humate, sodium starch glycolate and crospovidone. The direct compression approach was used to develop carvedilol fast dissolving tablets with a 23-factorial design. The formulations were assessed for flow characteristics, drug compatibility using FTIR, DSC and XRD, morphology using a scanning electron microscope, amount of drug, in vitro and in vivo drug release profiles and stability. Results: The modified starch-starch humate has a higher viscosity, pH value, and better flowability than sorghum starch. FTIR and DSC investigations revealed no interaction with the drug and the superdisintegrants. Optimized CARV-FDTs with 5% starch humate demonstrated adequate friability (0.59±0.68%), disintegration time (28±0.02 sec), % PD10 (98.40±0.64%), wetting time (22±0.36 sec), water absorption ratio (68±1.41) and DE (70.9±0.34). They also demonstrated satisfactory stability under accelerated conditions along with improved relative bioavailability, reaching the highest plasma concentration in a short time. Conclusion: This study discovered that modified starch humate can potentially be extracted and developed into fast dissolving tablets by QbD in the management of hypertension exhibiting enhanced relative bioavailability and patient acceptance.
Keywords
Subject
Article metadata
| Title | Optimized Formulation of Carvedilol Fast-Dissolving Tablets Using Modified Super disintegrants: Breaking Solubility Barriers of BCS Class II Drugs |
|---|---|
| Authors | Anilkumar Vadaga; Santosh Kumar Rada |
| Affiliations | Department of Pharmaceutics, GITAM School of Pharmacy, GITAM (Deemed to be University), Rushikonda, Visakhapatnam, Andhra Pradesh, INDIA.; Department of Pharmaceuitcs, School of Pharmacy, Godavari Global University, Rajahmundry, East Godavari, Andhra Pradesh, INDIA. |
| Corresponding author | anilvadaga@gmail.com |
| Journal | Indian Journal of Pharmaceutical Education and Research |
| Volume / Issue | Vol. 60, Issue 3 (2026) |
Also in this issue
- The Interplay between Traumatic Brain Injury, Cocaine Abuse, and Genetic Mutations in the Development of Parkinsons Disease: A Reviewpp. 918–924
- Utilizing Biomimetic Polymers for Innovations in Drug and Gene Deliverypp. 925–936
- Newer Pedagogical Methods for Teaching and Learning in Pharmaceutical Educationpp. 937–945
- Therapeutic Repurposing Strategies for Cardiovascular Disease Managementpp. 946–955
- Stimuli-Responsive and Functionalized Nanosponges: Precision Delivery to the Tumor Microenvironmentpp. 956–966
Readers Also Viewed
Effect of the Fractions of Coccinia grandis on Ethanol- Induced Cerebral Oxidative Stress in Rats
M. Umamaheswari, T. K. Chatterjee
Jan 1, 2009
Phytochemical Screening and Antioxidant Activity Evaluation of Selected Philippine Fruit Peels and Pulps
Mildred Dagcuta Pates, Angelo Mark Po Walag, Romeo M. Del Rosario
Aug 17, 2026
Impact of Artificial Intelligence Assisted Drug Therapy Optimization on Drug Related Problems Amongst Older Adult Patients: A Systematic Review
Jehath Syed, Christy Thomas, Bavneet Kaur
Oct 23, 2026