Follow the latest scientific research, product developments and company announcements concerning Bacospore®.
A peer-reviewed study in the International Journal of Basic and Applied Sciences evaluated B. coagulans MTCC 25308 with three other probiotic Bacillus strains. MTCC 25308 demonstrated the strongest DPPH activity of the four (IC₅₀ 54.19 µg/mL), high cellular viability, and moderate anti-adipogenic activity in 3T3-L1 cells.
A research study on Bacospore® MTCC 25308 reported approximately 80.4% inhibition of ethanol-induced ulcer formation, 26.6% diarrhoea inhibition at 200 mg/kg, 85.40% collagenase inhibition at 200 µg/mL and 97.72% cholesterol reduction at 1,000 µg/mL across animal and in-vitro models.
Star Hi Herbs issued the Bacospore® 300B specification: a standardized B. coagulans probiotic powder with ≥300 billion viable spores/g, water-soluble, GMO-free, BSE/TSE-free, non-irradiated and not treated with ethylene oxide.
International Journal of Basic and Applied Sciences, 15(2), 105–110. Four strains compared across cell viability, lipid accumulation, DPPH scavenging, PPAR-γ expression and α-amylase / α-glucosidase inhibition.
International Journal of Basic & Clinical Pharmacology (in press). Manuscript evaluates Bacospore® in gastrointestinal, extracellular-matrix and cholesterol reduction models.
Taxonomy of this spore-forming probiotic and why documents may use Heyndrickxia coagulans, Weizmannia coagulans or the former Bacillus coagulans.
How resistant endospores help B. coagulans tolerate heat, acid and gastrointestinal transit for shelf stability and intestinal delivery.
A practical guide covering viable-count calculations, moisture control and processing considerations.
Why CFU/g, overage, finished-product shelf life and storage conditions are critical when selecting a spore-forming probiotic.
Gastric mucosal protection, diarrhoea models and possible mechanisms involving barrier integrity, microbial balance and inflammatory modulation.
In-vitro evidence on cholesterol assimilation, bile interactions and BSH-associated mechanisms, and the distinction from human outcomes.
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