Related Experiment Video
Updated: Jun 12, 2026

Measuring Oral Fatty Acid Thresholds, Fat Perception, Fatty Food Liking, and Papillae Density in Humans
Published on: June 4, 2014
Cariogenicity and acidogenicity of human milk, plain and sweetened bovine milk: an in vitro study
A R Prabhakar1, Ameet J Kurthukoti, Pranjali Gupta
1Dept of Pedodontics and Preventive Dentistry, Bapuji Dental College and Hospital, Davanagere - 577004, Karnataka, India. attiguppeprabhakar@yahoo.com
Unlabelled:
The objective of the present study was to determine the acidogenicity and cariogenicity of human breast milk and plain and sweetened packaged bovine milk.
Study Design:
First all milk specimens were inoculated with a cariogenic strain of Streptococcus mutans (SM). The culture pH and number of colony forming units (cfus) was assessed. Second, the buffer capacity of all milk specimens was evaluated by mixing with acid. Finally, enamel windows were created on extracted primary maxillary incisors and colonized with SM. Enamel demineralization and caries progression were assessed visually, histologically, and radiographically at the end of twelve weeks.
Results:
Plain and sweetened packaged bovine milk (BM) supported greater bacterial growth and caused more fermentation than human breast milk (HBM). The buffer capacity values for plain and sweetened bovine milk were highest; HBM, however had poor buffering capacity. The progression of the carious lesions into the dentin was most severe for the sweetened bovine milk.
Conclusions:
HBM and plain bovine milk are relatively cariogenic in an in vitro caries model in the absence of saliva. However, supplementation with sugar exponentially enhances the cariogenic potential of the natural milk.
Related Concept Videos
Development of Human Microbiota
Acidity of Carboxylic Acids
Acidity and Basicity of Carboxylic Acid Derivatives
The relative acidic strength of the derivatives can be explained based on the extent of resonance stabilization of the conjugate base. The...
Microbes in Food Production
Production of Organic Acids
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives

