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
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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.

      128 023
      Development of a specific and sensitive high‑performance thin‑layer chromatography assay method for the determination of linagliptin in tablet dosage form
      V. RODE*, M. TAJNE (*Department of Pharmaceutical Sciences, Rashtrasant Tukadoji Maharaj Nagpur University, Nagpur, MS 440 033, India, vanitaashtankar10@gmail.com)

      J. Planar Chromatogr. 34, 279-283 (2021). HPTLC of linagliptin on silica gel with toluene - methanol 7:3. Quantitative determination by absorbance measurement at 294 nm. The hRF value for linagliptin was 91. Linearity was between 100 and 500 ng/zone. Intermediate precisions were below 2 % (n=3). The LOD and LOQ were 0.26 and 0.78 ng/zone, respectively. Recovery was between 99.1 % and 101.2 %.

      Classification: 32a
      128 020
      Study of the degradation behavior of dapagliflozin propanediol monohydrate and metformin hydrochloride by a stability‑indicating high‑performance thin‑layer chromatographic method
      Jasmina SURATI*, V. PATEL (*Department of Quality Assurance, Shree Naranjibhai Lalbhai Patel College of Pharmacy, Gujarat Technological University, Umrakh, Surat, Gujarat, India, j.s.surati@gmail.com)

      J. Planar Chromatogr. 34, 243-252 (2021). HPTLC of dapagliflozin (1) and metformin (2) on silica gel with methanol - ethyl acetate - ammonium acetate 60:40:1. Quantitative determination by absorbance measurement at 220 nm. The hRF values for (1) and (2) were 79 and 31, respectively. Linearity was between 20 and 100 ng/zone for (1) and 500 and 2500 ng/zone for (2), respectively. Intermediate precisions were below 2 % (n=5). The LOD and LOQ were 3 and 10 ng/zone for (1) and 11 and 34 ng/zone for (2), respectively. Recovery was between 100.0 % and 101.6 % for (1) and 99.7 % and 101.1 % for (2).

      Classification: 32a
      127 035
      Stability assessment of tamsulosin and tadalafil co-formulated in capsules by two validated chromatographic methods
      M. REZK, E. MOETY, M. WADIE*, M. TANTAWY (*Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, KasrEl-Aini Street, ET-11562, Cairo, Egypt, mina.wa.yousif@pharma.cu.edu.eg)

      J. Sep. Sci. 44, 530-538 (2021). HPTLC of tamsulosin (1) and tadalafil (2) in presence of their degradation products (2) and (3) on silica gel with ethyl acetate - toluene - methanol - ammonia 20:10:20:3. Quantitative determination by absorbance measurement at 280 nm. The hRF values for (1) to (4) were 55, 68, 14 and 24, respectively. Linearity was between 0.5 and 25 µg/zone for (1) and (2). Intermediate precision was below 2 % (n=3). Average recovery was 99.7 % for (1) and 100.3 % for (2).

      Classification: 23e, 32a
      127 041
      Simultaneous estimation of azilsartan medoxomil and chlorthalidone by chromatography method using design of experiment and quality risk management based quality by design approach
      P. PRAJAPATI*, S. PATEL, A. MISHRA (*Department of Quality Assurance, Maliba Pharmacy College, Uka Tarsadia University, Tarsadi, Mahuva, Surat, Gujarat 394350, India, pintu.prajapati@utu.ac.in)

      J. Planar Chromatogr. 33, 631-646 (2020). HPTLC of azilsartan medoxomil (1) and chlorthalidone (2) on silica gel with toluene - methanol - ethyl acetate - formic acid 35:10:5:1. Quantitative determination by absorbance measurement at 241 nm. The hRF values for (1) and (2) were 55 and 36. Linearity was between 800 and 4000 ng/zone for (1) and 250 and 1250 ng/zone for (2), respectively. Intermediate precision was below 2 % (n=3). The LOD and LOQ were 15 and 44 ng/zone for (1) and 10 and 32 ng/zone for (2). Recovery was between 100.8 and 101.7 % for (1) and 99.4 and 101.0 % for (2).

      Classification: 23e, 32a
      127 069
      Green HPLC–DAD and HPTLC methods for quantitative determination of binary mixture of pregabalin and amitriptyline used for neuropathic pain management
      I.A. NAGUIB, N.A. ALI*, F.A. ELROBY, M.R. ELGHOBASHY (*Anal. Toxicol. Lab., Forensic Med. Authority, Ministry of Justice, Cairo 11647, Egypt, n.aboyazeed@yahoo.com)

      J. of Chromatogr. Sci. 59 (6), 536-547 (2021). HPTLC of pregabalin (PGB) and amitriptyline (AMT) as an active binary mixture in pure forms or in human biological fluids (plasma/urine)  on silica gel with ethanol - ethyl acetate - acetone - ammonia solution 160:40:20:1. Detection by spraying with 3 % ethanolic ninhydrin solution. Quantitative determination by densitometry at 220 nm for AMT and 550 nm for PGB peaks after derivatization. The linearity range was 0.2 - 2.5 μg/band for PGB and 0.1-2.0 μg/band for AMT.

      Classification: 32a
      127 070
      Development and validation of two novel chromatographic methods: HPTLC and HPLC for determination of bromhexine hydrochloride in presence of its two impurities
      N.S. ABDELWAHAB, SELVIA M. ADLY*, N.W. ALI,MAHA M. ABDELRAHMAN (*Pharm. Anal. Chem. Dep., Faculty of Pharmacy, Beni-Suef Univ., Alshaheed Shehata Ahmed Hegazy St., Beni-Suef 62514, Egypt, selvia.maged.adly@gmail.com)

      J. of Chromatogr. Sci. 59(5), 425–431 (2021). HPTLC of bromhexine hydrochloride (BHX), impurity B (IMB) and impurity C (IMC) on silica gel with hexane - acetone - ammonia solution 450:25:4. Quantitative determination by densitometry at 240 nm. The linearity was in the range of 0.40-10.00, 0.20-2.00 and 0.20-2.00 μg/band for BHX, IMB and IMC, respectively. Comparison with an HPLC method showed no significant differences regarding accuracy and precision.

      Classification: 32a
      127 071
      Simultaneous determination of paracetamol, propyphenazone and caffeine in presence of paracetamol impurities using dual-mode gradient HPLC and TLC densitometry methods
      H. IBRAHIM*, A.M. HAMDY, H.A. MEREY, A.S. SAAD (*Anal. Chem. Dep., , Fac. of Pharmacy, Egyptian Russian Univ., Cairo-Suez Road, Badr City 11829, Egypt, hany.ibrahim@eru.edu.eg)

      J. of Chromatogr. Sci. 59 (2), 140-147 (2021). TLC of paracetamol (PC), propyphenazone (PZ) and caffeine (CF) in the presence of the two PC impurities 4-aminophenol and 4-nitrophenol, on silica gel with chloroform - toluene - ethyl acetate - methanol - acetic acid 60:60:10:20:1. Quantitative determination by densitometry at 220 nm.

      Classification: 32a
      127 074
      Optimization and validation of HPTLC method for estimation of ulipristal acetate in presence of its forced degradation products
      G. KAMDAR, S. DESAI* (*Dep. of Qual. Assur., SSR Coll. of Pharm., SSR Campus, Sayli Road, Silvassa 396 230, India, sdesai6381@gmail.com)

      J. of Chromatogr. Sci. 58 (5), 427 - 432 (2020). HPTLC of ulipristal acetate (UPA) in presence of its degradation products on silica gel with ethyl acetate - toluene - glacial acetic acid 40:70:3. UPA was subjected to acid and alkali hydrolysis, oxidation, photo and thermal degradation. The hRF of UPA was 38. Quantitative determination by densitometry. The linearity range was between 400-3600 ng/band. LOD was 72 ng/band and LOQ 220 ng/band. The recovery was 100.1-100.7 %. The method is accurate, precise, robust, and specific to measure UPA in presence of degradants.

       

      Classification: 32a