Cumulative CAMAG Bibliography Service CCBS
Our CCBS database includes more than 11,000 abstracts of publications. Perform your own detailed search of TLC/HPTLC literature and find relevant information.
The Cumulative CAMAG Bibliography Service CCBS contains all abstracts of CBS issues beginning with CBS 51. The database is updated after the publication of every other CBS edition. Currently the Cumulative CAMAG Bibliography Service includes more than 11'000 abstracts of publications between 1983 and today. With the online version you can perform your own detailed TLC/HPTLC literature search:
- Full text search: Enter a keyword, e.g. an author's name, a substance, a technique, a reagent or a term and see all related publications
- Browse and search by CBS classification: Select one of the 38 CBS classification categories where you want to search by a keyword
- Keyword register: select an initial character and browse associated keywords
- Search by CBS edition: Select a CBS edition and find all related publications
Registered users can create a tailor made PDF of selected articles throughout CCBS search – simply use the cart icon on the right hand of each abstract to create your individual selection of abstracts. You can export your saved items to PDF by clicking the download icon.
Chinese J. Pharm.Anal. (Yaowu Fenxi Zazhi) 10, 12-15 (1990). TLC of levamisole on silica with chloroform - toluene - acetone 7:5:2. Detection under UV 254 nm. Quantification by densitometry at 238 nm. Detection limit 3.0 nmol/mL.
Anal. Letters 25, 485-496 (1992). TLC of nicotine on silica with A) chloroform - methanol - acetic acid 11:8:1 and B) chloroform - methanol acetic acid 17:2:1. Quantification by densitometry at 262 nm.
Chromatographia 36, 293-296 (1993). Study of the effectiveness of 3-glycidoxypropyltreated TLC plates in the determination midazolam intoxication by TLC/fast atom bombardment MS. TLC of midazolam with chloroform. Identification of midazolam intoxication by TLC/FAB-MS, after applying the technique of diffused spot condensation on the plates. Improvement of the detection limit for midazolam in the serum of intoxication patient by 30 times.
J. Chromatogr. 668, 21-29 (1995). TLC of 73As-radiolabelled title compounds in aqueous solution, rat liver cytosol and urine of mice on cellulose with 1) methanol - NH3 8:2, 2) isopropanol - acetic acid - water 20:2:5. Detection by autoradiography. Oxidation of samples by hydrogen peroxide improved the separation and quantification of monomethylarsonate in both biological matrices.
J. Chromatogr. B 694, 443-447 (1997). HPTLC on silica with chloroform - methanol - NH3 20% 24:22:15. Detection by immersion into 0.25 mg/mL methanolic 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-Cl) and heating at 120°C for 10 min, and redevelopment with methanol. Quantification by fluorodensitometry at 436 nm. Precision < 2.8%, recovery 92.9 ± 1.74% (n=5).
Chinese J. Pharm. Anal. (Yaowu Fenxi Zazhi) 18, 153-156 (1998). TLC on silica gel with 1) chloroform - methanol 9:1 and 2) chloroform - toluene - ethanol 10:15:1. Detection by spraying with potassium iodobismuthate. Quantitation by densitometry at 305 nm. Precision within plate 3.27% (n=6), and plate-to-plate 5.39% (n=3). Recovery 80.0 ± 2.04% (n=5).
J. Planar Chromatogr. 14, 130-133 (2001). OPLC of formaldemethone (formaldehyde-dimedone adduct) on silica gel with chloroform - dichloromethane 2:6, protected from air. Quantitation by densitometry at 265 nm.
J. Chromatogr. B 823 (2), 152-157 (2005). HPTLC of lamotrigine (extracted from serum by ethyl acetate) on silica with toluene - acetone - ammonia 14:6:1. Densitometric measurement at 312 nm, hRf of lamotrigine at 54. The analytical method has excellent linearity (r = 0.998) in the range of 20–300 ng/spot. This assay range is adequate for analyzing human serum, as it corresponds to lamotrigine concentrations measured in human serum from epileptic patients. The method was validated for sensitivity, selectivity, extraction efficiency, accuracy and intra and inter-day reproducibility. The limit of detection and limit of quantification were found to be 6.4 and 10.2 ng, respectively. Good accuracy and high precision (CV) is reported, i.e. in the range of 92.1-97.1 % and 0.5-2.6 % respectively. The method was applied for determination of serum lamotrigine levels in epileptic patients and in pharmacokinetic study of lamotrigine administered orally to rabbits.