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Merck
모든 사진(1)

Key Documents

SAE0149

Sigma-Aldrich

Artificial Saliva for Pharmaceutical Research

동의어(들):

Artificial Saliva Solution, Saliva Substitute

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About This Item

UNSPSC 코드:
51241229
NACRES:
NA.25

배송 상태

wet ice

저장 온도

2-8°C

일반 설명

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.

애플리케이션

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

성분

Sodium Chloride
Potassium Phosphate Monobasic
Potassium Chloride
Potassium Thiocyanate Urea

저장 및 안정성

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

Storage Class Code

12 - Non Combustible Liquids

WGK

nwg

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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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