Evidence map›Paper›PMID 42366292›Full record

ArticleDaru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences2026

Chitosan-carboxymethyl tara gum polyelectrolyte complex matrix tablets for sustained gastrointestinal drug dissolution using paracetamol as a model drug.

Md Sahil Shanawaz Alam, Tapan Kumar Giri, Kaushik Mukherjee

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Article in Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

3 authors.

Md Sahil Shanawaz AlamDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata, India.
Tapan Kumar GiriDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata, India.
Kaushik MukherjeeDepartment of Pharmaceutical Technology, Jadavpur University, Kolkata, India. kaushik.pharmacyju08@gmail.com.ORCID https://orcid.org/0009-0009-3490-8707

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNatural polysaccharides are extensively used for delivery of bioactives because of its eco-friendly, biocompatible and biodegradable characteristics. However, substantial swelling and poor rheological characteristics limits its applications as drug carriers for sustained delivery.

objectiveChitosan (CTS) and carboxymethyl tara gum (CMTG) matrix tablets were unable provide sustained drug dissolution owing to substantial swelling and low viscosity of the matrix. The present research embarks on the development of CTS and CMTG polyelectrolyte complex (PEC) matrix tablets for sustained gastrointestinal drug dissolution.

methodsPECs of CTS and CMTG were prepared by one shot addition method. The formation of the PECs was optimized in terms of % yield, FTIR, turbidity analysis, zeta potential, viscosity, and swelling studies. The PEC matrix tablets were prepared by wet granulation method.

resultsAt a fixed concentration of CMTG, increasing CTS concentration led to the formation of non-stoichiometric PECs with reduced % yield and poor mechanical strength making it unsuitable for tableting. At a fixed concentration of CTS, progressive increase in the concentration of CMTG resulted in the formation of stoichiometric PECs which improved the % yield and viscosity, lowered swelling index and had sufficient mechanical strength to be tableted. PEC matrix tablet F7 prepared with optimized PEC 7 (ratio between CTS and CMTG 1:3) released only 40% drug after 12 h of dissolution.

conclusionPending validation through in vivo and stability studies, we conclude that CTS- CMTG PEC matrix tablets can be a suitable matrix material for sustained gastrointestinal drug dissolution.

Indexed as

AcetaminophenChitosanPlant GumsDelayed-Action PreparationsDrug CarriersDrug LiberationSolubilityTabletsViscosityAcetaminophenChitosanDelayed-Action PreparationsDrug CarriersPlant GumsTabletsCarboxymethyl tara gumChitosanMatrix tabletsPolyelectrolyte complexSustained drug dissolution

Identifiers

PMID42366292
PMCPMC13310873

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.