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Efficient protection of microorganisms for delivery to the intestinal tract by cellulose sulphate encapsulation.
Gunzburg, Walter H; Aung, Myo Myint; Toa, Pauline; Ng, Shirelle; Read, Eliot; Tan, Wee Jin; Brandtner, Eva Maria; Dangerfield, John; Salmons, Brian.
Affiliation
  • Gunzburg WH; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore. gunzburg@sgaustria.com.
  • Aung MM; Institute of Virology, Department of Pathobiology, University of Veterinary Medicine, 1210, Vienna, Austria. gunzburg@sgaustria.com.
  • Toa P; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore.
  • Ng S; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore.
  • Read E; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore.
  • Tan WJ; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore.
  • Brandtner EM; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore.
  • Dangerfield J; Austrianova Singapore, 41 Science Park Road, #03-15 The Gemini, Singapore, 117610, Singapore.
  • Salmons B; VIVIT - Vorarlberg Institute for Vascular Investigation and Treatment, Feldkirch, Austria.
Microb Cell Fact ; 19(1): 216, 2020 Nov 26.
Article in En | MEDLINE | ID: mdl-33243224
BACKGROUND: Gut microbiota in humans and animals play an important role in health, aiding in digestion, regulation of the immune system and protection against pathogens. Changes or imbalances in the gut microbiota (dysbiosis) have been linked to a variety of local and systemic diseases, and there is growing evidence that restoring the balance of the microbiota by delivery of probiotic microorganisms can improve health. However, orally delivered probiotic microorganisms must survive transit through lethal highly acid conditions of the stomach and bile salts in the small intestine. Current methods to protect probiotic microorganisms are still not effective enough. RESULTS: We have developed a cell encapsulation technology based on the natural polymer, cellulose sulphate (CS), that protects members of the microbiota from stomach acid and bile. Here we show that six commonly used probiotic strains (5 bacteria and 1 yeast) can be encapsulated within CS microspheres. These encapsulated strains survive low pH in vitro for at least 4 h without appreciable loss in viability as compared to their respective non-encapsulated counterparts. They also survive subsequent exposure to bile. The CS microspheres can be digested by cellulase at concentrations found in the human intestine, indicating one mechanism of release. Studies in mice that were fed CS encapsulated autofluorescing, commensal E. coli demonstrated release and colonization of the intestinal tract. CONCLUSION: Taken together, the data suggests that CS microencapsulation can protect bacteria and yeasts from viability losses due to stomach acid, allowing the use of lower oral doses of probiotics and microbiota, whilst ensuring good intestinal delivery and release.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cellulose / Drug Delivery Systems / Probiotics / Drug Compounding / Escherichia coli / Cell Encapsulation Limits: Animals / Humans / Male Language: En Journal: Microb Cell Fact Journal subject: BIOTECNOLOGIA / MICROBIOLOGIA Year: 2020 Document type: Article Affiliation country: Singapore Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cellulose / Drug Delivery Systems / Probiotics / Drug Compounding / Escherichia coli / Cell Encapsulation Limits: Animals / Humans / Male Language: En Journal: Microb Cell Fact Journal subject: BIOTECNOLOGIA / MICROBIOLOGIA Year: 2020 Document type: Article Affiliation country: Singapore Country of publication: United kingdom