Journals / Marmara Pharmaceutical Journal / 2017 / Cilt: 21 - Sayı: 4

Interpenetrating networks of carboxymethyl tamarind gum and chitosan for sustained delivery of aceclofenac

Pages
771–782
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

From the results, it can be concluded that the IPNs of CMTG and chitosan has potential in development of site specific sustained drug delivery.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:The aim of present investigation was to characterize carboxymethyl tamarind gum (CMTG) based interpenetrating networks (IPNs) of aceclofenac for site specific sustained delivery.
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Key Findings & Data:The IPNs were characterized by Attenuated total reflectanceFourier transform infrared (ATR-FTIR) spectroscopy, thermal analysis, X-ray powder diffraction and solid state 13C-nuclear magnetic resonance spectroscopy.
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Conclusion & Impact:From the results, it can be concluded that the IPNs of CMTG and chitosan has potential in development of site specific sustained drug delivery.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

The aim of present investigation was to characterize carboxymethyl tamarind gum (CMTG) based interpenetrating networks (IPNs) of aceclofenac for site specific sustained delivery. The drug loaded IPNs were prepared by using chitosan and CMTG as polymers and gluteraldehyde as crosslinking agent. The IPNs were characterized by Attenuated total reflectanceFourier transform infrared (ATR-FTIR) spectroscopy, thermal analysis, X-ray powder diffraction and solid state 13C-nuclear magnetic resonance spectroscopy. The prepared IPNs were evaluated for the drug entrapment efficiency and equilibrium swelling. The drug release from IPNs was studied in 0.1NHCl for 2h followed by phosphate buffer pH 6.8 for further 10h and compared with commercial tablet. The results of ATR-FTIR and thermal analysis for blank IPNs indicated intercalation of polymeric chains of crosslinked CMTG and chitosan. The results of solid state characterization revealed that the aceclofenac is compatible with IPNs. Entrapment efficiency of IPNs was found to be increased with increase in crosslinker concentration as well as amount of CMTG. The equilibrium swelling study indicated pH dependent swelling of IPNs. The drug release by IPNs showed sustained release of aceclofenac upto 12h while commercial formulation showed fast release within 8h. From the results, it can be concluded that the IPNs of CMTG and chitosan has potential in development of site specific sustained drug delivery.

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Cite This Article

MALI, K. K., DHAWALE, S. C., DIAS, R. J., HAVALDAR, V. D., KAVITAKE, P. R. (2017). Interpenetrating networks of carboxymethyl tamarind gum and chitosan for sustained delivery of aceclofenac. Marmara Pharmaceutical Journal, Cilt: 21 - Sayı: 4, 771–782. https://ajindex.com/articles/283698

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References (11)

  1. Costa P, Sousa Lobo JM. Modeling and comparison of dissolution profiles. Eur J Pharm Sci 2001;13:123–33.
  2. Seki Y, Altinisik A, Demircioğlu B, Tetik C. Carboxymethylcellulose (CMC)-hydroxyethylcellulose (HEC) based hydrogels: Synthesis and characterization. Cellulose 2014;21:1689–98.
  3. Sannino A, Maffezzoli A, Nicolais L. Introduction of molecular spacers between the crosslinks of a cellulose-based superabsorbent hydrogel: Effects on the equilibrium sorption properties. J Appl Polym Sci 2003;90:168–74.
  4. Ghorpade VS, Yadav AV, Dias RJ. Citric acid crosslinked β-cyclodextrin/carboxymethylcellulose hydrogel films for controlled delivery of poorly soluble drugs. Carbohydr Polym 2017;164:339–48.
  5. Deshmukh RK, Naik JB. Aceclofenac microspheres: Quality by design approach. Mater Sci Eng C. 2014;36:320–8.
  6. Suresh S, Gunasekaran S, Srinivasan S. Studies of the molecular geometry, vibrational spectra, frontier molecular orbital, nonlinear optical and thermodynamics properties of aceclofenac by quantum chemical calculations. Spectrochim Acta A Mol Biomol Spectrosc 2014;125:239–51.
  7. Distantina S, Rochmadi, Fahrurrozi M, Wiratni. Preparation of hydrogel based on glutaraldehyde-crosslinked carrageenan. 3rd International Conference on Chemistry and Chemical Engineering 2012;38:150–4.
  8. Balaji R, Raghunathan S, Revathy R. Levofloxacin: formulation and in-vitro evaluation of alginate and chitosan nanospheres. Egypt Pharm J 2015;14:30. Jana S, Gandhi A, Sheet S, Sen KK. Metal ion-induced alginatelocust bean gum IPN microspheres for sustained oral delivery of aceclofenac. Int J Biol Macromol 2015;72:47–53.
  9. Kulkarni RV, Mangond BS, Mutalik S, Sa B. Interpenetrating polymer network microcapsules of gellan gum and egg albumin entrapped with diltiazem-resin complex for controlled release application. Carbohydr Polym 2011;83:1001–7.
  10. Jana S, Das A, Nayak AK, Sen KK, Basu SK. Aceclofenac-loaded unsaturated esterified alginate/gellan gum microspheres: In vitro and in vivo assessment. Int J Biol Macromol 2013;57:129– 37. Trivedi JH. Synthesis, characterization, and swelling behavior of superabsorbent hydrogel from sodium salt of partially carboxymethylated tamarind kernel powder-g-PAN. J Appl Polym Sci 2013;129:1992–2003.
  11. Sanyasi S, Majhi RK, Kumar S, Mishra M, Ghosh A, Suar M, Satyam PV, Mohapatra H, Goswami C, Goswami L. Polysaccharide-capped silver Nanoparticles inhibit biofilm formation and eliminate multi-drug-resistant bacteria by disrupting bacterial cytoskeleton with reduced cytotoxici