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58469AST

Supelco

CHIRALPAK® HSA (5 μm) HPLC Columns

L × I.D. 5 cm × 3 mm, HPLC Column

同義詞:

Chiral HSA Analytical Column

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About This Item

分類程式碼代碼:
41115700
eCl@ss:
32110501
NACRES:
SB.52

product name

CHIRAL-HSA 高效液相色谱柱, 5 μm particle size, L × I.D. 5 cm × 3 mm

材料

stainless steel column

agency

suitable for USP L79

產品線

CHIRALPAK®

包裝

pkg of 1 ea

製造商/商標名

CHIRALPAK®

參數

137 bar pressure (2000 psi)
20-30 °C temperature
40 °C max. temp.

技術

HPLC: suitable

長度 × 內徑

5 cm × 3 mm

基質

fully porous particle

基質活性組

human serum albumin phase

粒徑

5 μm

工作pH值

2-8

分離技術

chiral

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一般說明

CHIRALPAK HSA, which uses human serum albumin as the chiral selector, is highly selective for acidic racemates, preferably weak and strong acids, zwitterionic and non-protolytic (neutral) compounds. Phosphate buffers (normally 0.01-0.1M, pH 5-7) with addition of organic modifiers are used as mobile phases. Enantioselectivity and retention can be regulated by changing the mobile phase composition. However, the primary use of CHIRALPAK HSA is for fast drug/protein binding studies (1). To calculate the % protein binding, measure the retention time of an unretained compound (t0) and the compound of interest (tr) on the CHIRALPAK HSA column. Then use the capacity factor equation:
k = (tr - t0)/tr
to calculate the % protein binding (P):
P = 100k/(k+1)

Different types of mobile phases can be used. A mobile phase consisting of 6% 2-propanol in 20 mM potassium phosphate buffer, pH 7.0 gives data in good agreement with literature data. The mobile phase conditions should be chosen to suit the drugs to be tested, i.e., for high protein binding drugs a mobile phase with higher eluting strength might be needed in order to reduce retention times.

(1) Goodman, A.; Gilman, A.G. The Pharmacological Basis of Therapeutics, 9th Edition, McGraw-Hill: New York, 1996; pp 1712-1792.

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法律資訊

CHIRALPAK is a registered trademark of Daicel Corp.

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