Enhancement of the immediate release of paracetamol from alginate beads

Objective: Alginate beads are not soluble in the acid leading to small portion released in the stomach. This may not be favourable for drugs administered for fast action like paracetamol. So, this study was aimed to increase the immediate release of paracetamol from alginate beads, i.e. the release...

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Bibliographic Details
Main Authors: Alfatama, M. (Author), Ayob, F.A (Author), Doolaanea, A.A (Author), Hamed, S. (Author)
Format: Article
Language:English
Published: Innovare Academics Sciences Pvt. Ltd 2017
Subjects:
Online Access:View Fulltext in Publisher
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LEADER 03095nam a2200445Ia 4500
001 10.22159-ijap.2017v9i2.15672
008 220120s2017 CNT 000 0 und d
020 |a 09757058 (ISSN) 
245 1 0 |a Enhancement of the immediate release of paracetamol from alginate beads 
260 0 |b Innovare Academics Sciences Pvt. Ltd  |c 2017 
520 3 |a Objective: Alginate beads are not soluble in the acid leading to small portion released in the stomach. This may not be favourable for drugs administered for fast action like paracetamol. So, this study was aimed to increase the immediate release of paracetamol from alginate beads, i.e. the release in the acidic pH. Methods: The beads were prepared by dropwise paracetamol/alginate suspension in divalent cation solution. Two attempts were used to increase the dissolution of paracetamol in the acidic pH. First attempt was by only changing preparation variables: needle size, alginate viscosity and drug loading using 23 full factorial design. The second approach was by adding excipients like carbopol, tween and polyethylene glycol. The beads were characterized for their size, encapsulation efficiency and release profile. Results: First approach, changing preparation variables without excipient adding, helped to increase the drug release in the acid but to a maximum of 26% using a smaller needle, lower drug loading and higher alginate viscosity. However, optimising the formulation with suitable excipients increased the drug release in the acid to 77.3%. The optimised formulation included carbopol 940 (pH sensitive polymer) and tween 80 (facilitates water entry) in the beads, with using barium chloride instead of calcium chloride together with PEG 400 in the complexing solution. Conclusion: To achieve immediate release of paracetamol from alginate beads in the acidic pH, excipients need to be added. Rational selection of excipients is critical to achieve the desired drug release. © 2016 The Authors. 
650 0 4 |a acidity 
650 0 4 |a Alginate beads 
650 0 4 |a alginic acid 
650 0 4 |a Article 
650 0 4 |a barium chloride 
650 0 4 |a calcium chloride 
650 0 4 |a carbomer 
650 0 4 |a controlled study 
650 0 4 |a drug delivery system 
650 0 4 |a drug release 
650 0 4 |a drug solubility 
650 0 4 |a drug synthesis 
650 0 4 |a encapsulation 
650 0 4 |a Excipients 
650 0 4 |a Factorial design 
650 0 4 |a Immediate release 
650 0 4 |a macrogol 
650 0 4 |a macrogol 400 
650 0 4 |a paracetamol 
650 0 4 |a Paracetamol 
650 0 4 |a particle size 
650 0 4 |a viscosity 
700 1 0 |a Alfatama, M.  |e author 
700 1 0 |a Ayob, F.A.  |e author 
700 1 0 |a Doolaanea, A.A.  |e author 
700 1 0 |a Hamed, S.  |e author 
773 |t International Journal of Applied Pharmaceutics  |x 09757058 (ISSN)  |g 9 2, 47-51 
856 |z View Fulltext in Publisher  |u https://doi.org/10.22159/ijap.2017v9i2.15672 
856 |z View in Scopus  |u https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019857719&doi=10.22159%2fijap.2017v9i2.15672&partnerID=40&md5=2e836bb4c327827ea815b71f7321884e