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Key Documents

SAE0149

Sigma-Aldrich

Artificial Saliva for Pharmaceutical Research

Synonyme(s) :

Artificial Saliva Solution, Saliva Substitute

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About This Item

Code UNSPSC :
51241229
Nomenclature NACRES :
NA.25

Conditions d'expédition

wet ice

Température de stockage

2-8°C

Description générale

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.

Application

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

Composants

Sodium Chloride
Potassium Phosphate Monobasic
Potassium Chloride
Potassium Thiocyanate Urea

Stockage et stabilité

This is a ready to use formulation that should be stored refrigerated.

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

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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