Probiotic survival during a multi-layered tablet development as tested in a dynamic, computer-controlled in vitro model of the stomach and small intestine (TIM-1).
Bifidobacterium
Lactobacillus
TIM-1
multi-layered tablet
probiotic
survival
Journal
Letters in applied microbiology
ISSN: 1472-765X
Titre abrégé: Lett Appl Microbiol
Pays: England
ID NLM: 8510094
Informations de publication
Date de publication:
Nov 2019
Nov 2019
Historique:
received:
07
02
2019
revised:
08
08
2019
accepted:
09
08
2019
pubmed:
28
8
2019
medline:
21
12
2019
entrez:
28
8
2019
Statut:
ppublish
Résumé
The aim of the research was to develop a galenical formulation for the combination of the three probiotic strains Lactobacillus gasseri PA 16/8, Bifidobacterium longum SP 07/3 and Bifidobacterium bifidum MF 20/5 that would lead to the presence of a high amount of viable cells in the small intestine, the presumed site of action of these strains. This was tested in a validated, dynamic in vitro model of the stomach and small intestine (TIM-1), simulating human adults after intake of a meal. Experiments were performed both in the gastric compartment of the model, as well as in the complete system (stomach + small intestine). Survival of the strains in an unformulated probiotic powder after transit through the gastric compartment was 5·3% for the bifidobacteria and 1% for L. gasseri. After transit through the complete gastrointestinal tract, this dropped to 2% for bifidobacteria and 0·1% for Lactobacillus. After several rounds of optimization, an enteric-coated tablet was developed that increased the delivery of viable cells reaching the small intestine to 72% (gastric survival) for bifidobacteria, and 53% (gastric) for L. gasseri. Also survival in the small intestine increased by about an order of magnitude. The final galenical formulation was tested in two applications: adults and elderly, both of which have their own physiological parameters. These experiments corroborated the results obtained in the development phase of the project. In conclusion, the developed enteric coating led to a 20- to 40-fold increase in the delivery of viable cells to the small intestine. SIGNIFICANCE AND IMPACT OF THE STUDY: Predictive GI in vitro models are very helpful and reliable tools for the development of new galenical formula containing probiotics, and in the current example helped to deliver >10-fold higher numbers of viable cells to the small intestine, presumably leading to improved functionality of the strains.
Identifiants
pubmed: 31454425
doi: 10.1111/lam.13211
pmc: PMC6856813
doi:
Substances chimiques
Tablets
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
325-332Subventions
Organisme : Merck Selbsmedikation GmbH , Darmstadt, Germany
ID : not applicable
Informations de copyright
© 2019 The Authors. Letters in Applied Microbiology published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology.
Références
Benef Microbes. 2015;6(2):159-65
pubmed: 25576593
Benef Microbes. 2017 May 30;8(3):491-496
pubmed: 28504581
Microb Cell Fact. 2011 Aug 30;10 Suppl 1:S19
pubmed: 21995734
Benef Microbes. 2012 Sep;3(3):229-36
pubmed: 22968412
Pharm Res. 2012 Jun;29(6):1444-53
pubmed: 22068280
Benef Microbes. 2017 Apr 26;8(2):323-325
pubmed: 28403650
Adv Biochem Eng Biotechnol. 2008;111:1-66
pubmed: 18461293
Gut Pathog. 2017 Mar 6;9:12
pubmed: 28286570
Br J Nutr. 2010 Apr;103(7):1079-81
pubmed: 20230653
J Am Coll Nutr. 2015;34(6):459-69
pubmed: 25909149
J Dairy Sci. 1997 Jun;80(6):1031-7
pubmed: 9201571
Am J Clin Nutr. 2017 Mar;105(3):758-767
pubmed: 28228426
Drug Dev Ind Pharm. 2007 Apr;33(4):475-83
pubmed: 17523011
Eur J Pharm Sci. 2006 Jan;27(1):72-9
pubmed: 16169713
Clin Nutr. 2005 Aug;24(4):481-91
pubmed: 16054520
Food Microbiol. 2017 Sep;66:20-27
pubmed: 28576369
Vaccine. 2006 Nov 10;24(44-46):6670-4
pubmed: 16844267
Int J Food Microbiol. 2011 Sep 15;149(2):152-8
pubmed: 21741105
Nat Rev Gastroenterol Hepatol. 2014 Aug;11(8):506-14
pubmed: 24912386
Invest Radiol. 1999 May;34(5):357-9
pubmed: 10226848
J Appl Microbiol. 2018 Jun;124(6):1604-1609
pubmed: 29473976