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Chitosan based in situ forming polyelectrolyte complexes: A potential sustained drug delivery polymeric carrier for high dose drugs.
Mater Sci Eng C Mater Biol Appl. 2017 Oct 01; 79:491-498.MS

Abstract

The present study investigated the feasibility of using combination of Cationic and anionic polymers as sustained release carrier for the delivery of high dose gastric acid soluble model drug Paracetamol. Various formulations were prepared using wet granulation technique. Briefly a cooled (4°C) neutral solution of chitosan (CH) was combined with cooled aqueous solution (4°C) of anionic polymer such as Gum Ghatti (GG) and Xanthan gum (XG). This polyelectrolyte solution was then used to granulate the model drug Paracetamol. The prepared tablets were evaluated for various pharmacopoeial and non pharmacopoeial parameters viz. Thickness, Hardness, Friability, Weight Variation, Content uniformity and Drug Content. The drug release study carried out in 0.1M HCl revealed in situ Polyelectrolyte complex formation (PEC) between CH and anionic biopolymers. This in situ PEC formation resulted in sustained delivery of high dose gastric fluid soluble drug Paracetamol. Further, effect of incorporation starch and lactose as tablet diluents on release rate was also studied. It was observed that paracetamol release from lactose granulation was faster than tablets prepared with starch as diluents. From the data generated it was concluded that In situ PEC formation approach has sufficient potential to sustain the release of drugs like paracetamol.

Authors+Show Affiliations

Department of Pharmaceutics, School of Pharmaceutical Sciences, IFTM University, Moradabad, Uttar Pradesh, 244001, India. Electronic address: niharikalal24@gmail.com.Department of Pharmaceutics, School of Pharmaceutical Sciences, IFTM University, Moradabad, Uttar Pradesh, 244001, India.Department of Pharmaceutics, I.T.S. Paramedical College (Pharmacy), Muradnagar, Ghaziabad, Uttar Pradesh, 201206, India.Department of Pharmaceutics, School of Pharmaceutical Sciences, IFTM University, Moradabad, Uttar Pradesh, 244001, India.Department of Pharmaceutics, School of Pharmaceutical Sciences, IFTM University, Moradabad, Uttar Pradesh, 244001, India. Electronic address: anuragverma_iftm@yahoo.co.in.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28629045

Citation

Lal, Niharika, et al. "Chitosan Based in Situ Forming Polyelectrolyte Complexes: a Potential Sustained Drug Delivery Polymeric Carrier for High Dose Drugs." Materials Science & Engineering. C, Materials for Biological Applications, vol. 79, 2017, pp. 491-498.
Lal N, Dubey J, Gaur P, et al. Chitosan based in situ forming polyelectrolyte complexes: A potential sustained drug delivery polymeric carrier for high dose drugs. Mater Sci Eng C Mater Biol Appl. 2017;79:491-498.
Lal, N., Dubey, J., Gaur, P., Verma, N., & Verma, A. (2017). Chitosan based in situ forming polyelectrolyte complexes: A potential sustained drug delivery polymeric carrier for high dose drugs. Materials Science & Engineering. C, Materials for Biological Applications, 79, 491-498. https://doi.org/10.1016/j.msec.2017.05.051
Lal N, et al. Chitosan Based in Situ Forming Polyelectrolyte Complexes: a Potential Sustained Drug Delivery Polymeric Carrier for High Dose Drugs. Mater Sci Eng C Mater Biol Appl. 2017 Oct 1;79:491-498. PubMed PMID: 28629045.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Chitosan based in situ forming polyelectrolyte complexes: A potential sustained drug delivery polymeric carrier for high dose drugs. AU - Lal,Niharika, AU - Dubey,Juhi, AU - Gaur,Praveen, AU - Verma,Navneet, AU - Verma,Anurag, Y1 - 2017/05/10/ PY - 2016/11/24/received PY - 2017/04/29/revised PY - 2017/05/10/accepted PY - 2017/6/21/entrez PY - 2017/6/21/pubmed PY - 2018/3/6/medline KW - Chitosan KW - Diluent KW - Gum Ghatti KW - Polyelectrolyte complex KW - Xanthan gum SP - 491 EP - 498 JF - Materials science & engineering. C, Materials for biological applications JO - Mater Sci Eng C Mater Biol Appl VL - 79 N2 - The present study investigated the feasibility of using combination of Cationic and anionic polymers as sustained release carrier for the delivery of high dose gastric acid soluble model drug Paracetamol. Various formulations were prepared using wet granulation technique. Briefly a cooled (4°C) neutral solution of chitosan (CH) was combined with cooled aqueous solution (4°C) of anionic polymer such as Gum Ghatti (GG) and Xanthan gum (XG). This polyelectrolyte solution was then used to granulate the model drug Paracetamol. The prepared tablets were evaluated for various pharmacopoeial and non pharmacopoeial parameters viz. Thickness, Hardness, Friability, Weight Variation, Content uniformity and Drug Content. The drug release study carried out in 0.1M HCl revealed in situ Polyelectrolyte complex formation (PEC) between CH and anionic biopolymers. This in situ PEC formation resulted in sustained delivery of high dose gastric fluid soluble drug Paracetamol. Further, effect of incorporation starch and lactose as tablet diluents on release rate was also studied. It was observed that paracetamol release from lactose granulation was faster than tablets prepared with starch as diluents. From the data generated it was concluded that In situ PEC formation approach has sufficient potential to sustain the release of drugs like paracetamol. SN - 1873-0191 UR - https://www.unboundmedicine.com/medline/citation/28629045/Chitosan_based_in_situ_forming_polyelectrolyte_complexes:_A_potential_sustained_drug_delivery_polymeric_carrier_for_high_dose_drugs_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0928-4931(16)32341-4 DB - PRIME DP - Unbound Medicine ER -