SAE0149
Artificial Saliva for Pharmaceutical Research
Sinónimos:
Artificial Saliva Solution, Saliva Substitute
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About This Item
Código UNSPSC:
51241229
NACRES:
NA.25
Productos recomendados
Condiciones de envío
wet ice
temp. de almacenamiento
2-8°C
Descripción general
Artificial saliva helps in gaining a stable environment and standardized procedures for in vitro and in vivo studies in pharmacological and bioengineering fields. This saliva mimics the properties of natural saliva in terms of chemical composition and physical characteristics. Artificial Saliva is formulated according to literature for pharmaceutical research such as studies of drug dissolution and drug delivery through the oral mucosa.
Aplicación
Artificial Saliva for pharmaceutical research has been used:
- to study the antifungal activity of Candida albicans on the surface of printed denture resin discs
- as a diluting agent for inactivation of Escherichia coli in droplets are with different ambient humidities
- to determine the stability of graphene oxide-amoxicillin (GO-AMOX) capsules
Componentes
Sodium Chloride
Potassium Phosphate Monobasic
Potassium Chloride
Potassium Thiocyanate Urea
Potassium Phosphate Monobasic
Potassium Chloride
Potassium Thiocyanate Urea
Almacenamiento y estabilidad
This is a ready to use formulation that should be stored refrigerated.
Código de clase de almacenamiento
12 - Non Combustible Liquids
Clase de riesgo para el agua (WGK)
nwg
Punto de inflamabilidad (°F)
Not applicable
Punto de inflamabilidad (°C)
Not applicable
Certificados de análisis (COA)
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J J Pytko-Polonczyk et al.
Journal of physiology and pharmacology : an official journal of the Polish Physiological Society, 68(6), 807-813 (2018-03-20)
Examination of dental materials and their properties at the initial stage of the digestive process requires the development of conditions that mimic the environment of the oral cavity. One of the main components of this area is saliva, where many
Anna Trusek et al.
Materials (Basel, Switzerland), 14(12) (2021-07-03)
Graphene oxide (GO) was proposed as an efficient carrier of antibiotics. The model drug, amoxicillin (AMOX), was attached to GO using a peptide linker (Leu-Leu-Gly). GO-AMOX was dispersed in a hydrogel to which the enzyme responsible for releasing AMOX from
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