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.
J. Planar Chromatogr. 32, 481-493 (2019). HPTLC of metformin hydrochloride (1) and ursodeoxycholic acid (2) on silica gel with toluene - ethanol - acetone - formic acid 90:40:50:17. Quantitative determination by absorbance measurement at 234 and 700 nm for (1) and (2), respectively. The hRF values for (1) and (2) were 19 and 80, respectively. Linearity was between 5000 and 40000 ng/zone for (1) and 1500 and 12000 ng/zone for (2). Intermediate precision was below 1 % (n=3). The LOD and LOQ were 195 and 592 ng/zone for (1) and 150 and 455 ng/zone for (2), respectively. Recovery rate was 100.5 % for (1) and 99.9 % for (2).
J. Planar Chromatogr. 32, 501-504 (2019). HPTLC of aspirin (1) and omeprazole (2) on silica gel with ethyl acetate - dichloromethane - glacial acetic acid 80:20:1. Quantitative determination by absorbance measurement at 241 nm. The hRF values for (1) and (2) were 79 and 19, respectively. Linearity was between 160 and 960 ng/zone for (1) and 80 and 480 ng/zone for (2). Intermediate precision was below 1 % (n=3). The LOD and LOQ were 11 and 32 ng/zone for (1) and 3 and 8 ng/zone for (2), respectively. Recovery rate was between 101 and 106 % for both (1) and (2).
J. Planar Chromatogr. 32, 517-520 (2019). HPTLC of tramadol (1), caffeine (2), paracetamol (3), ibuprofen (4), naproxen (5), and diclofenac (6) on RP-18 WF, LiChrospher RP-18 WF, and RP-18 WF with concentration zone, developed with various ratios of methanol in water with 0.1 M potassium chloride. Qualitative identification under UV light at 254 nm. Potassium chloride may be used to suppress ion–ion interactions between the solutes and the silica gel surface. HPTLC RP-18WF plates with concentration zone and developed with methanol - water 13:7 with addition of 0.15 mol/L KCl were suitable for the qualitative and quantitative analyses of tramadol, paracetamol, caffeine, naproxen, and ibuprofen or diclofenac. The method allowed to study subtle differences in the efficiency of the separation of analgesic drugs by HPTLC with similar octadecyl silica-based adsorbents.
J. Planar Chromatogr. 32, 411-420 (2019). HPTLC of fosinopril sodium (1), hydrochlorothiazide (2), and chlorothiazide (3) on silica gel with ethyl acetate - chloroform - methanol - formic acid 120:80:10:1. Quantitative determination by absorbance measurement at 215 nm. The hRF values for (1) to (3) were 53, 39 and 29, respectively. Linearity was between 1 and 10 µg/zone for (1), 0.2 and 3 µg/zone for (2) and 0.2 and 2 µg/zone for (3). Intermediate precisions were below 2 % (n=6). The LOD and LOQ were 280 and 860 ng/zone for (1), 90 and 350 ng/zone for (2) and 50 and 160 ng/zone for (3). Recovery rate was 100.2 % for (1), 100.1 % for (2) and 99.9 % for (3).
J. AOAC Int. 102, 776-780 (2019). HPTLC of sibutramine, phenolphthalein, and three PDE5 inhibitors (sildenafil, vardenafil and tadalafil), as well as caffeine, fluoxetine, theophylline, and acetaminophen as adulterants in weight loss products on silica gel with methyl tert-butyl ether – toluene – methanol 8:2:1. Densitometric absorption measurement at 225 nm. The hRF values of reference substances increased in the following order: fluoxetine, sildenafil, vardenafil, caffeine, theophylline, tadalafil, acetaminophen, phenolphthalein and sibutramine. The method was successfully used for the screening of 12 commercial products. Of those, nine products tested positive for at least one undeclared component.
J. Liq. Chromatogr. Relat. Technol. 42, 324-329 (2019). HPTLC of individual pharmaceutical products containing moxifloxacin HCl (1), ofloxacin (2), amoxicillin trihydrate (3), acetylsalicylic acid + acetaminophen + caffeine (4), nimesulide (5), irbesartan (6), and pantoprazole (7) on silica gel with methanol - ammonium hydroxide - water 7:2:1 for (1), methanol - ethyl acetate - ammonium hydroxide 7:7:3 for (2), acetone - water - methanol - glacial acetic acid 20:10:5:2 for (3), ethyl acetate - glacial acetic acid 19:1 for (4), toluene - acetone 10:1 for (5), ethyl acetate - acetone - glacial acetic acid 180:40:1 for (6) and ethyl acetate - methanol - toluene 4:1:2 for (7). Quantitative determination by absorbance measurement at 366 nm. The hRF values for (1) to (3) and (5) to (7) were 72, 30, 80, 33, 40 and 43, respectively. The hRF values for (4) were 62 for acetylsalicylic acid, 49 for acetaminophen and 22 for caffeine. The quantitative methods were used to transfer the Global Pharma Health Fund (GPHF) Minilab Manual and U.S. Food and Drug Administration (FDA) Compendium to HPTLC following a model process for moxfloxacin HCl, ofloxacin, and amoxicillin trihydrate. The results met the guidelines of the model process regarding the calibration curves: r-values were at least 0.99, assays were within 85–115% specification limits of the label values of individual tablets and capsules, validation recoveries were within 95 - 105 % at all three spike levels, RSDs were no higher than 3 % for assays and validation analyses, and peak identity and peak purity checks had correlation factors of at least
0.99.
J. Liq. Chromatogr. Relat. Technol. 42, 238-248 (2019). Review of recent applications of TLC in medicinal chemistry, including the determination of lipophilicity of biologically active compounds and its influence as activity descriptors of absorption, distribution, metabolism, elimination and toxicity. Practical applications of TLC as a fast screening technique in different stages of monitoring processes were also described, including systems recently used for stability studies of selected drugs.
J. Planar Chromatogr. 32, 273-283 (2019). HPTLC of trimetazidine dihydrochloride (1) and its potential impurities, namely, piperazinecarboxaldehyde (2), trimethoxybenzyl alcohol (3), and trimethoxybenzaldehyde (4) on RP-18 with acetonitrile - methanol - 0.1 % aqueous ortho-phosphoric acid (pH 6.2) 9:9:2. Quantitative determination by absorbance measurement at 254 nm. The hRF values for (1) to (4) were 21, 35, 50 and 85, respectively. Linearity was between 0.05-10 µg/zone for (1), 0.05-1.1 µg/zone for (2), 0.05-1.2 µg/zone for (3) and 0.04-1.0 µg/zone for (4). The intermediate precision was below 2 % (n=9). The LOD and LOQ were 20 and 50 ng/zone for (1) to (3) and 15 and 40 ng/zone for (4), respectively. Recovery rate was 99.6 % for (1), 100.5 % for (2), 100.1 % for (3) and 99.4 % for (4).