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. 26, 427-434 (2013). HPTLC of oseltamivir (1) in pharmaceuticals counterfeited with ascorbic acid (2) on silica gel with methanol - water 3:2 +1 drop ammonia. Quantitative determination by absorbance measurement at 254 nm. The hRf values for (1) and (2) were 70 and 83, respectively. Linearity was between 5 and 14 µg/zone. LOD and LOQ were 2 and 5 µg/zone. Average recovery (by standard addition) was found to be 100.6 %. Intermediate intra- and inter-day precision was below 1.6 %. Comparing with colorimetric method, HPTLC method provided advantages in terms of speed, lower cost, and environmental protection without sacrificing accuracy.
J. Chromatogr. A 1289, 105-118 (2013). HPTLC of 11 anthocyanes named cyanidin (1), delphinidin (2), malvidin (3), peonidin (4), pelargonidin (5), cyanidin-3-glucoside (6), delphinidin-3-glucoside (7), malvidin-3-glucoside (8), peonidin-3-glucoside (9), pelargonidin-3-glucoside (10) and malvidin-3,5-diglucoside (11) in pomace, feed, juice and wine on silica gel with ethyl acetate - toluene - formic acid - water 50:15:4:6 for the anthocyanidins (1) to (5) and ethyl acetate - 2-butanone - formic acid - water 35:15:6:4 for the anthocyanins (6) to (11). Quantitative determination by absorbance measurement using a multi-wavelength scan at 505 nm for (10), 510 nm for (5), 520 nm for (4) and (9), 530 nm for (1), (3), (6), (8) and (11) and 555 nm for (7). Detection was compared by dipping into a DPPH radical reagent solution (0.5 mM methanolic solution of the DPPH) and into Aliivibrio fischeri bioassay suspension. Linearity was in the range of 180-540 ng/zone for (1), 47-141 ng/zone for (2), 147-441 ng/zone for (3), 24-89 ng/zone for (4), 32-95 ng/zone for (5), 71-343 ng/zone for (6), 63-304 ng/zone for (7), 40-191 ng/zone for (8), 27-131 ng/zone for (9), 16-76 ng/zone for (10) and 45-219 ng/zone for (11). The intermediate precision over several months was below 6.7 % (n=3). The LODs of the anthocyanidins were much better compared to those for anthocyanins. The LOQs for (1) to (11) were below 90 ng/zone, most even below 30 ng/zone and for (9) and (10), the LOQ were even below 7 ng/zone. Radical scavenging as well as bioactivity properties were important complementary detection methods.
J. Planar Chromatogr. 27, 210-216 (2014). HPTLC of 5-hydroxy-L-tryptophan (1), 5-methyltryptamine (2), L-tryptophan (3) and melatonin (4) on silica gel with propan-2-ol - 25 % ammonia - water 8:1:1. Quantitative determination by absorbance measurement at 280 nm. The hRF values for (1) to (4) were 47, 79, 53 and 85, respectively. Linearity was in the range of 48-720 µg/zone for (1), 38-646 µg/zone for (2), 100-2000 µg/zone for (3) and 108-1737 µg/zone for (4). The intermediate/interday/intra-day precisions were below 3 % (n=5). The LOD and LOQ were 16 and 49 ng/zone for (1), 40 and 122 ng/zone for (2), 116 and 352 ng/zone for (3) and 145 and 439 ng/zone for (4). Mean recovery was between 97.4 and 100.1 % for (1) to (4).
J. Planar Chromatogr. 27, 66-68 (2014). TLC of profenofos in visceral tissues on silica gel with n-hexane - acetone 4:1. Detection by spraying with 10 % sodium hydroxide solution and after 5-10 min, spraying with diazotized sulfanilic acid reagent (0.5 g sulfanilic acid and 1 g sodium nitrite in 100 mL of 10 % v/v hydrochloric acid). The hRF value for profenofos was 45.
J. Planar Chromatogr. 27, 52-57 (2014). HPTLC of paracetamol (1), dicyclomine hydrochloride (2) and mefenamic acid (3) on silica gel with toluene - ethyl acetate - methanol 6:3:1. Quantitative determination by absorbance measurement at 290 nm. The hRF values for (1) to (3) were 27, 41 and 61, respectively. Linearity was in the range of 600-1800 ng/zone for (1), 400-2400 ng/zone for (2) and 300-1500 ng/zone for (3). The intermediate/interday/intra-day precisions were below 2 % (n=3). The LOD and LOQ were 35 and 116 ng/zone for (1), 109 and 360 ng/zone for (2) and 42 and 140 ng/zone for (3), respectively. Recovery was in the range of 97.7-99.9 % for (1) to (3).
J. Planar Chromatogr. 28, 54-60 (2015). HPTLC of bergenin in the aerial parts of Flueggea virosa on silica gel with dichloromethane – methanol 17:3. Quantitative determination by absorbance measurement at 220 nm. The hRF value of bergenin was 29. Linearity was between 100 and 800 ng/zone. The intermediate intra-day and inter-day precisions were below 2 % (n=6). The LOD and LOQ for bergenin were 18 and 53 ng/zone, respectively. Recoveries were in the range of 99-100 %.
J. Planar Chromatogr. 27, 438-443 (2014). HPTLC of (1) alpha-amyrin, (2) lupeol, and (3) beta-sitosterol in the leaves of Kalanchoe pinnata, Bombax ceiba, and Morus alba on silica gel with toluene – ethyl acetate 19:1. Detection by dipping into anisaldehyde–sulphuric acid reagent for 1 min, followed by heating at 100 °C for 5 min. Quantitative determination by absorbance measurement at 525 nm. The hRF values of (1) to (3) were 71, 28 and 16 respectively. Linearities were in the range of 160-560 ng/zone for (1), 150-900 ng/zone for (2) and 80-480 ng/zone for (3). The intermediate precision was below 2 % (n=3) for (1) to (3). The LOD and LOQ were 60 and 160 ng/zone for (1), 50 and 150 ng/zone for (2) and 20 and 48 ng/zone for (3), respectively. Average recoveries for (1) to (3) were 100.7, 99.8 and 100.1 %, respectively.
J. Planar Chromatogr. 27, 377-384 (2014). HPTLC of metformin in urine on silica gel with chloroform – methanol – ammonia 27 % 25:25:1. Quantitative determination by absorbance measurement at 237 nm. The hRF value of metformin was 25. Linearity was between 200 and 2000 ng/zone. The intermediate inter-day and intra-day precisions were below 9 % (n=5). The LOD and LOQ were 40 and 120 ng/zone, respectively. Recoveries were in the range of 92-94 %.