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. 2018 May 31:2018:1459849.
doi: 10.1155/2018/1459849. eCollection 2018.

Cocoa Pod Husk Pectin Intended as a Pharmaceutical Excipient Has No Adverse Effects on Haematological Parameters in Sprague Dawley Rats

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Cocoa Pod Husk Pectin Intended as a Pharmaceutical Excipient Has No Adverse Effects on Haematological Parameters in Sprague Dawley Rats

Ofosua Adi-Dako et al. J Pharm (Cairo). .

Abstract

Natural polymer research has recently become the focus of intensive research in the quest for new enabling excipients for novel drugs in pharmaceutical formulation for optimal treatment outcomes. Evaluations of some excipients have shown deleterious haematological effects of varying extents on the safety profile of these excipients. A 90-day subchronic toxicity study was conducted to evaluate the influence of cocoa pod husk (CPH) pectin on indicators for haematotoxicity. Male and female Sprague Dawley rats (SDRs) were fed with CPH pectin in doses up to 71.4 mg/kg. The effects of CPH pectin on the haematological indices, direct and total bilirubin, and the spleen were determined. The results indicated that CPH pectin did not induce any untoward toxic effects on the haematological indices, bilirubin levels, and the spleen. There were, however, elevations in MCV at day 30, which was not sustained after the 90 days. The data obtained from this study did not reveal any remarkable findings of toxicological relevance to the haematopoietic system.

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Figures

Figure 1
Figure 1
The effect of varying dose levels of CPH pectin on the histology of the spleen of female SDRs (magnification, ×400).

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References

    1. Ogaji I. J., Nep E. I., Audu-Peter J. D. Advances in natural polymers as pharmaceutical excipients. Pharmaceutica Analytica Acta. 2012;3, article 146 doi: 10.4172/2153-2435.1000146. - DOI
    1. Pifferi G., Santoro P., Pedrani M. Quality and functionality of excipients. Farmaco. 1999;54(1-2):1–14. doi: 10.1016/S0014-827X(98)00101-3. - DOI - PubMed
    1. Forman S. A. Clinical and molecular pharmacology of etomidate. Anesthesiology. 2011;114(3):695–707. doi: 10.1097/aln.0b013e3181ff72b5. - DOI - PMC - PubMed
    1. Beneke C. E., Viljoen A. M., Hamman J. H. Polymeric plant-derived excipients in drug delivery. Molecules. 2009;14(7):2602–2620. doi: 10.3390/molecules14072602. - DOI - PMC - PubMed
    1. Coviello T., Matricardi P., Marianecci C., Alhaique F. Polysaccharide hydrogels for modified release formulations. Journal of Controlled Release. 2007;119(1):5–24. doi: 10.1016/j.jconrel.2007.01.004. - DOI - PubMed

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