Recombinant biologic products versus nutraceuticals from plants - a regulatory choice?
- PMID: 27297459
- PMCID: PMC5338133
- DOI: 10.1111/bcp.13041
Recombinant biologic products versus nutraceuticals from plants - a regulatory choice?
Abstract
Biotechnology has transformed the potential for plants to be a manufacturing source of pharmaceutical compounds. Now, with transgenic and transient expression techniques, virtually any biologic, including vaccines and therapeutics, could be manufactured in plants. However, uncertainty over the regulatory path for such new pharmaceuticals has been a deterrent. Consideration has been given to using alternative regulatory paths, including those for nutraceuticals or cosmetic agents. This review will consider these possibilities, and discuss the difficulties in establishing regulatory guidelines for new pharmaceutical manufacturing technologies.
Keywords: GMP; manufacturing; monoclonal antibody; recombinant pharmaceutical; transgenic plants.
© 2016 The British Pharmacological Society.
References
-
- Gurib‐Fakim A. Medicinal plants: traditions of yesterday and drugs of tomorrow. Mol Aspects Med 2006; 27: 1–93. - PubMed
-
- Raskin I, Ribnicky DM, Komarnytsky S, Ilic N, Poulev A, Borisjuk N, et al. Plants and human health in the twenty‐first century. Trends Biotechnol 2002; 20: 522–31. - PubMed
-
- Paul MJ, Thangaraj H, Ma JK. Commercialization of new biotechnology: a systematic review of 16 commercial case studies in a novel manufacturing sector. Plant Biotechnol J 2015; 13: 1209–20. - PubMed
-
- Ma JK, Drossard J, Lewis D, Altmann F, Boyle J, Christou P, et al. Regulatory approval and a first‐in‐human phase I clinical trial of a monoclonal antibody produced in transgenic tobacco plants. Plant Biotechnol J 2015; 13: 1106–20. - PubMed
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