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.
Food Chem. 351, 129211 (2021). High-throughput planar solid-phase extraction of 66 multi-class antibiotic residues in muscle tissue, cow milk and chicken eggs on silica gel with acetonitrile - methanol - ammonia 5:3:2 as first front-elution up to 85 mm followed by a second front-elution in the reverse direction up to 25 mm with acetonitrile -water - ammonia 9:7:4. Evaluation under UV 254 nm and 366 nm. Detection of macrolides by spraying with p-anisaldehyde sulfuric acid reagent (methanol - glacial acetic acid - sulfuric acid - p–anisaldehyde 420:50:26:3), followed by heating at 110°C for 3 min. Detection of penicillins by spraying with ninhydrin reagent (500 mg ninhydrin in ethanol - glacial acetic acid 23:2). Detection of lincosamines by spraying with aniline diphenylamine o-phosphoric acid reagent (2 g diphenylamine in methanol – o-phosphoric acid - aniline 90:10:1). Via simple clicks on the image, the auto TLC-MS interface automatically eluted the target zones at the trace level from the TLC plate into a Q Exactive Plus Hybrid Quadrupole-Orbitrap Mass Spectrometer.
J. Liq. Chromatogr. Relat. Technol. https://doi.org/10.1080/10826076.2021.1968429 (2021). Review of bioautography procedures of antimicrobial compounds in plants, including extraction of plant material, stationary and mobile phases in direct bioautography, chemical derivatization and biological detection of bioactive compounds and structure elucidation of bioactive bands. The paper also discussed new aspects of identification of biologically active substances in accordance with the principles of green analytical chemistry, and with special reference to substances with antimicrobial properties.
J. Liq. Chromatogr. Relat. Technol. https://doi.org/10.1080/10826076.2021.1930556 (2021). HPTLC of patulin in apple juice on silica gel with methyl tert-butylether - n-pentane 9:5. Detection by spraying with 0.25 % methyl-benzothiazolinone hydrazone hydrochloride monohydrate in methanol, followed by heating at 105 °C. Quantification was performed using a 48-bit flatbed scanner for color measurements (in red, green, and blue). Quantification in fluorescence mode by use of a 16-bit CCD-camera and UV-366 nm illumination as well as a HPTLC DAD-scanner. The hRF value for patulin was 58. Linearity was between 5 and 800 ng/zone. The LOD and LOQ were 33 and 67 ng/zone, respectively.
J. Liq. Chromatogr. Relat. Technol. https://doi.org/10.1080/10826076.2021.1930555 (2021). HPTLC of ofloxacin (1), tinidazole (2), terbinafine hydrochloride (3), and clobetasol propionate (4) on silica gel with toluene - ethyl acetate - methanol - triethylamine - formic acid 50:40:10:3:3. Quantitative determination by absorbance measurement at 238 nm. Linearity was between 300 and 1500 ng/zone for (1) to (4). The intermediate precision was below 2 % (n=6). Recovery was between 98.9 and 99.1 % for (1), 98.9 and 99.3 % for (2), 99.0 and 99.5 % for (3) and 98.9 and 99.3 % for (4).
Anal. Bioanal. Chem. 411, 6655-6665 (2019). HPTLC of lovastatin present in lactone (1) and hydroxy acid forms (2) and mycotoxin citrinin (3) in red yeast rice on silica gel with n-hexane - acetone - 10 % acetic acid 60:40:1. Quantitative determination by absorbance measurement at 238 nm for (1) and (2) and fluorescence measurement at 313/> 400 nm for (3). The hRF values for (1) to (3) were 35, 23 and 7, respectively. Linearity was between 50 and 500 ng/zone for (1) and (2) and 5 and 50 ng/zone for (3). Intermediate precision was below 2 % (n=5). The LOD and LOQ were 10 and 50 ng/zone for (1) and (2) and 1 and 4 ng/zone for (3). Average recovery was 109.9 % for (1) to (3).
J. AOAC Int. 103, 980-988 (2020). HPTLC of imidocarb dipropionate and its forced induced degradation products in bovine meat and milk on silica gel with ethyl acetate - methanol - ammonia - water 85:10:5:2. Quantitative determination by absorbance measurement at 254 nm. Linearity was between 100 and 1800 ng/zone. Intermediate precision was below 1 % (n=3). The LOD and LOQ were 17 and 52 ng/zone, respectively. Average recovery was 100.8 %. The HPTLC method showed comparable results to a validated HPLC method for resolution and determination of imidocarb in the presence of its degradation products.
J. Planar Chromatogr. 34, 121-129 (2021). HPTLC of cefoperazone (1) and sulbactam (2) on silica gel with acetone - ethanol - ethyl acetate - 2 % sodium dodecyl sulfate - glacial acetic acid 6:4:8:2:1. Quantitative determination by absorbance measurement at 265 nm. The hRF values for (1) and (2) were 45 and 69, respectively. Linearity was between 150 and 1000 ng/zone for (1) and 100 and 1000 ng/zone for (2). Intermediate precision was below 2 % (n=3). The LOD and LOQ were 42 and 129 ng/zone for (1) and 30 and 90 ng/zone for (2), respectively. Recovery was between 99.5 and 100.5 % for (1) and 99.1 and 100.4 % for (2).
J. Planar Chromatogr. 33, 617-630 (2020). HPTLC of aflatoxin B1 in marketed samples of corn, groundnut, rice, wheat and dried chillies on silica gel with chloroform - acetone 9:1. Quantitative determination by absorbance measurement at 366 nm. The hRF value for aflatoxin B1 was 36. Linearity was between 10 and 120 ng/zone. Intermediate precision was below 2 % (n=3). The LOD and LOQ were 1 and 3 ng/zone. Average recovery was 85.2 %.