Advances in the use of instrumental measurement of colour in the development, production and quality control of drugs, medicinal preparations and pharmaceutical auxiliary substances III

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    6. Šubert J., Čižmárik J. Pokroky ve využití instrumentálního měření barevnosti ve vývoji, výrobě a kontrole jakosti léčiv, léčivých přípravků a pomocných látek I. Čes. slov. Farm. 2013; 62, 65–70.

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    8. Miyazaki Y., Miyawaki K., Uchino T., Kagawa Y. Assessment of blending ratio of powdered medicine mixtures by image analysis. Chem. Pharm. Bull. 2014; 62, 322–327. https://doi.org/10.1248/cpb.c13-00772 (8. 2. 2020).

    9. Miyazaki Y., Uchino T., Kagawa Y. Evaluation of degree of blending colored diluents using color difference signal method. Chem. Pharm. Bull. 2014; 62, 488–490. https://doi.org/10.1248/cpb.c14-00020 (8. 2. 2020).

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  12. Quintanilla-Carvajal M. X., Hernández-Sánchez H., Alamilla-Beltrán L., Zepeda-Vallejo G., Jaramillo-Flores M. E., de Jesús Perea-Flores M., Jimennez-Aparicio A., Gutiérrez-López G. F. Effects of microfluidisation process on the amounts and distribution of encapsulated and non-encapsulated α-tocopherol microcapsules obtained by spray drying. Food Res. Int. 2014; 63, 2–8. https://doi.org/10.1016/j.foodres.2014.05.025 (22. 12. 2019).

  13. Moon J. S., Park M., Kim W. G., Kim C., Hwang J., Seol D., Kim C. S., Sohn J. R., Chung H., Oh J. W. M-13 bacteriophage based structural color sensor for detecting antibiotics. Sens. Actuators B: Chem. 2017; 240, 757–762. https://doi.org/10.1016/j.snb.2016.09.050 (26. 11. 2019).

  14. Gouda M. A., Eldien H. F., Girges M. M., Berghot M. A. Synthesis and antitumor evaluation of thiophene based azo dyes incorporating pyrazolone moiety. J. Saudi Chem. Soc. 2016; 20, 151–157. https://doi.org/10.1016/j.jscs.2012.06.004 (26. 11. 2019).

  15. Gaffer H., Salem M., Marzouk M. Synthesis of 4-hydroxy coumarin dyes and their applications. Pigment Resin Technol. 2016; 45, 320–329. https://doi.org/10.1108/PRT-09-2014-0071 (26. 11. 2019).

  16. Abu-Melha S. Synthesis of novel biologically active thiazole dyes and their applications. Pigment Resin Technol. 2019; 48, 375–382. https://doi.org/10.1108/PRT-09-2018-0102 (26. 11. 2019).

  17. Swartz T. E., Yin J., Patapoff T. W., Horst T., Skieresz S. M., Leggett G., Morgan C. J., Rahimi K., Marhoul J., Kabakoff B. A spectral method for color quantitation of a protein drug solution. PDA J. Pharm. Sci. Technol. 2016; 70, 361–381. https://doi.org/ 10.5731/pdajpst.2016.006486 (30. 6. 2016).

  18. Yin J., Swartz T. E., Zhang J., Patapoff T. W., Chen B., Marhoul J., Shih N., Kabakoff B., Rahimi K. Validation of a spectral method for quantitative measurement of color in protein drug solutions. PDA J. Pharm. Sci. Technol. 2016; 70, 382–391. https://doi.org/10.5731/pdajpst.2016.006494 (30. 6. 2016).

  19. Ragab H. S., El-Kader M. A. Optical and thermal studies of starch/methylcellulose blends. Phys. Scr. 2013; 87, 025602. http://dx.doi.org/10.1088/0031-8949/87/02/025602 (26. 11. 2019).

  20. Okonogi S., Kaewpinta A., Yotsawimonwat S., Khongkhun­thian S. Preparation and characterization of lidocaine rice gel for oral application. Drug Discov. Ther. 2015; 9, 397–403. https://doi.org/10.5582/ddt.2015.01065 (26. 11. 2019).

  21. Taylor T., Chouljenko A., Bonilla F., Scott R., Bueno F., Reyes V., Lanclos C., Calumba K. F., Sathivel S. A pectin-gelatin gel containing oral rehydration solution and the release of sodium chloride under simulated gastric conditions. Int. J. Biol. Macromol. 2019; 136, 1112–1118. https://doi.org/10.1016/j.ijbiomac.2019.06.146 (22. 12. 2019).

  22. Vukicevic M., Randeberg L. L., Boschker J. E., Tybell T., Tønnesen H. H. Influence of crystal modification on the photoinduced color change in riboflavin. Pharmazie 2014; 69, 117–124.

  23. Jutkus R. A., Li N., Taylor L. S., Mauer L. J. Effect of temperature and initial moisture content on the chemical stability and color change of various forms of vitamin C. Int. J. Food Properties 2015; 18, 862–879. https://doi.org/10.1080/10942912.2013.805770 (22. 12. 2019).

  24. Sanchez J. O., Ismail Y., Christina B., Mauer L. J. Degradation of L‐ascorbic acid in the amorphous solid state. J. Food Sci. 2018; 83, 670–681. https://doi.org/10.1111/1750-3841.13998 (22. 12. 2019).

  25. Teraoka R., Fukami T., Furuishi T., Nagase H., Ueda H., Tode C., Yutani R., Kitagawa S., Sakane T. Improving the solid-state photostability of furosemide by Its cocrystal formation. Chem. Pharm. Bull. 2019; 67, 940–944. https://doi.org/10.1248/cpb.c18-00812 (8. 2. 2020).

  26. Sreedhara A., Yin J., Joyce M., Lau K., Wecksler A. T., Deperalta G., Yi L., Wang J., Kabakoff B., Kishore R. S. Effect of ambient light on IgG1 monoclonal antibodies during drug product processing and development. Eur. J. Pharm. Biopharm. 2016; 100, 38–46. https://doi.org/10.1016/j.ejpb.2015.12.003 (22. 12. 2019).

  27. Mochizuki K., Takayama K. Prediction of color changes using the time-temperature superposition principle in liquid formulations. Chem. Pharm. Bull. 2014; 62, 1225–1230. https://doi.org/10.1248/cpb.c14-00530 (8. 2. 2020).

  28. Mochizuki K., Takayama K. Prediction of color changes in acetaminophen solution using the time–temperature superposition principle. Drug Dev. Ind. Pharm. 2016; 42, 1050–1057. https://doi.org/10.3109/03639045.2015.1107091 (2. 12. 2019).

  29. Kharat M., Du Z., Zhang G., Julian D., McClements D. J. Physical and chemical stability of curcumin in aqueous solutions and emulsions: Impact of pH, temperature, and molecular environment. J. Agric. Food Chem. 2017; 65, 1525–1532. https://doi.org/10.1021/acs.jafc.6b04815 (22. 5. 2019).

  30. Estanqueiro M., Conceição J., Amaral M. H., Lobo J. M. S. Use of solid dispersions to increase stability of dithranol in topical formulations. Braz. J. Pharm. Sci. 2014; 50, 583–590. http://dx.doi.org/10.1590/S1984-82502014000300018 (6. 12. 2019).

  31. Katsura S., Yamada N., Nakashima A., Shiraishi S., Gunji M., Furuishi T., Endo T., Ueda H., Yonemochi E. Investigation of discoloration of furosemide tablets in a light-shielded environment. Chem. Pharm. Bull. 2017; 65, 373–380. https://doi.org/10.1248/cpb.c16-00835 (8. 2. 2020).

  32. Fujisawa Y., Takahashi Y., Teraoka R., Kitagawa S. Photostability of risperidone in tablets. KONA Powder Part. J. 2018; 35, 209–215. https://doi.org/10.14356/kona.2018008 (6. 12. 2019).

  33. Bjerknes K., Helmizadeh Z., Brustugun J., Smistad G. Physical stability of moisture‐sensitive tablets stored in a canister or as a unit‐dose. J. Pharm. Pract. Res. 2017; 47, 442–448. https://doi.org/10.1002/jppr.1306 (7. 12. 2019).

  34. Barling D., Morton D. A., Hapgood, K. Pharmaceutical dry powder blending and scale-up: maintaining equivalent mixing conditions using a coloured tracer powder. Powder Technol. 2015; 270, 461–469. https://doi.org/10.1016/j.powtec.2014.04.069 (22. 12. 2019).

  35. Nguyen D., Rasmuson A., Thalberg K., Björn I. N. A study of the redistribution of fines between carriers in adhesive particle mixing using image analysis with coloured tracers. Powder Technol. 2016; 299, 71–76. https://doi.org/10.1016/j.powtec.2016.05.030 (22. 12. 2019).

  36. Šibanc R., Luštrik M., Dreu R. Analysis of pellet coating uniformity using a computer scanner. Int. J. Pharm. 2017; 533, 377–382. https://doi.org/10.1016/j.ijpharm.2017.06.016 (15. 12. 2019).

  37. Barimani S., Šibanc R., Kleinebudde P. Optimization of a semi-batch tablet coating process for a continuous manufacturing line by design of experiments. Int. J. Pharm. 2018; 539, 95–103. https://doi.org/10.1016/j.ijpharm.2018.01.038 (22. 12. 2019).

  38. Murillo M. A., Rodríguez‐Pulido F. J., Heredia F. J., Melgosa M., Pacheco J., Vargas R., Montero E., Gutiérrez D. Color evolution during a coating process of pharmaceutical tablet cores by random spraying. Color Res. Appl. 2019; 44, 160–167. https://doi.org/10.1002/col.22332 (22. 12. 2019).

  39. Yoshino H., Yamashita K., Iwao Y., Noguchi S., Itai S. Quantitative appearance inspection for film coated tablets. Chem. Pharm. Bull. 2016; 64, 1226–1229. https://doi.org/10.1248/cpb.c15-01030 (8. 2. 2020).

  40. Feng L., Xiaoyu L., Yi C. An efficient detection method for rare colored capsule based on RGB and HSV color space. In: 2014 IEEE International Conference on Granular Computing (GrC). Noboribetsu: IEEE 2014; 175–178. https://doi.org/10.1109/GRC.2014.6982830 (22. 12. 2019).

  41. Senthilnathan R., Ranjani R., Nandhini M., Nithya S. A color classification algorithm for vision based pallet inspection applicable in pharmaceutical industries. J. Chem. Pharm. Sci. 2016; 9, 3289–3295. https://pdfs.semanticscholar.org/4cb3/174da5c274b1f38bec0eb63ba67206ca0403.pdf) (20. 12. 2019).

  42. Vijayasankaran N., Varma S., Yang Y., Mun M., Arevalo S., Gawlitzek M., Swartz T., Lim A., Li F., Zhang B., Meier S., Kiss R. Effect of cell culture medium components on color of formulated monoclonal antibody drug substance. Biotechnol. Prog. 2013; 29, 1270–1277. https://doi.org/10.1002/btpr.1772 (22. 12. 2019).

  43. Derfus G. E., Dizon-Maspat J., Broddrick J. T., Velayo A. C., Toschi J. D., Santuray R. T., Hsu S. K., Winter C. M., Krishnan R., Amanullah A. Red colored IgG4 caused by vitamin B12 from cell culture media combined with disulfide reduction at harvest. MAbs 2014; 6, 679–688. https://doi.org/10.4161/mabs.28257 (22. 12. 2019).

  44. Song H., Xu J., Jin M., Huang C., Bongers J., Bai H., Wu W., Ludwig R., Li Z., Tao L., Das T. K. Investigation of color in a fusion protein using advanced analytical techniques: delineating contributions from oxidation products and process related impurities. Pharm. Res. 2016; 33, 932–941. https://doi.org/10.1007/s11095-015-1839-3 (22. 12. 2019).

  45. Chaplenko A. A., Monogarova O. V., Oskolok K. V. Using a molecular sensor array with colorimetric detection to identify active ingredients in drug formulations. Pharm. Chem. J. 2019; 53, 347–352. https//doi:10.1007/s11094-019-02004-0 (22. 12. 2019).

  46. Monogarova O. V., Chaplenko A. A., Oskolok K. V. Multisensory digital colorimetry to identify and determination of active substances in drugs. Sens. Actuators B: Chem. 2019; 299, 126909. https://doi.org/10.1016/j.snb.2019.126909 (22. 12. 2019).

  47. Al Hagbani T., Veronin M. A., Nutan M. T., Nazzal S. Can the surface color of pharmaceutical tablets be used as a unique product identifier? J. Drug Deliv. Sci. Tech. 2017; 37, 141–146. https://doi.org/10.1016/j.jddst.2016.12.010 (22. 12. 2019).

  48. Kumpanenko I. V., Roshchin A. V., Ivanova N. A., Bloshenko A. V., Shalynina N. A., Korneeva T. N. Colorimetry: Choice of colorimetric parameters for chromophore concentration measurements. Russ. J. Gen. Chem. 2014; 84, 2295–2304. https://doi.org/10.1134/S1070363214110498 (19. 1. 2020).

  49. Shokrollahi A., Ebrahimi F. Simultaneous determination of brilliant green and basic fuchsin by cloud point extraction–scanometry. J. Anal. Chem. 2019; 74, 1019–1026. https://doi.org/10.1134/S1061934819100101 (22. 12. 2019).

  50. Vakili H., Nyman J. O., Genina N., Preis M., Sandler N. Application of a colorimetric technique in quality control for printed pediatric orodispersible drug delivery systems containing propranolol hydrochloride. Int. J. Pharm. 2016; 511, 606–618. https://doi.org/10.1016/j.ijpharm.2016.07.032 (22. 12. 2019).

  51. Wickström H., Nyman J. O., Indola M., Sundelin H., Kronberg L., Preis M., Rantanen J., Sandler N. Colorimetry as quality control tool for individual inkjet-printed pediatric formulations. AAPS Pharm. Sci. Tech. 2017; 18, 293–302. https://doi.org/10.1208/s12249-016-0620-1 (22. 12. 2019).

  52. Alev-Tuzuner B., Beyler-Cigil A., Vezir Kahraman M., Yarat A. PEG-based hydrogel-coated test strip for on-site urea determination. Int. J. Polym. Mater. Polym. Biomater. 2019; 68, 597–606. https://doi.org/10.1080/00914037.2018.1482460 (22. 1. 2020).

  53. Ait Errayess S., Idrissi L., Amine A. Smartphone-based colorimetric determination of sulfadiazine and sulfasalazine in pharmaceutical and veterinary formulations. Instr. Sci. Technol. 2018; 46, 656–675. https://doi.org/10.1080/10739149.2018.1443943 (28. 1. 2020).

  54. Choodum A., Parabun K., Klawach N., Daeid N. N., Kanatharana P., Wongniramaikul W. Real time quantitative colourimetric test for methamphetamine detection using digital and mobile phone technology. Forensic Sci. Int. 2014; 235, 8–13. https://doi.org/ 0.1016/j.forsciint.2013.11.018 (22. 12. 2019).

  55. Kostelnik A., Cegan A., Pohanka M. Acetylcholinesterase inhibitors assay using colorimetric pH sensitive strips and image analysis by a smartphone. Int. J. Anal. Chem. 2017; Article ID 3712384. https://doi.org/10.1155/2017/3712384 (23. 1. 2020).

  56. Zou B., Liu Y., Yan X., Huang C. Gold nanoparticles based digital color analysis for quinidine detection. Chin. Sci. Bull. 2013; 58, 2027–2031. https://doi.org/10.1007/s11434-013-5708-3 (24. 1. 2020).

  57. Lodha A., Pandya A., Sutariya P. G., Menon S. K. A smart and rapid colorimetric method for the detection of codeine sulphate, using unmodified gold nanoprobe. RSC Adv. 2014; 4, 50443–50448. https://doi.org/10.1039/C4RA06269H (24. 1. 2020).

  58. Hemmateenejad B., Dorostkar S., Shakerizadeh-Shirazi F., Shamsipur M. pH-independent optical sensing of heparin based on ionic liquid-capped gold nanoparticles. Analyst 2013; 138, 4830–4837. https://doi.org/10.1039/C3AN36895E (24. 1. 2020).

  59. Ping J., He Z., Liu J., Xie X. Smartphone‐based colorimetric chiral recognition of ibuprofen using aptamers‐capped gold nanoparticles. Electrophoresis 2017; 39, 486–495. https://doi.org/10.1002/elps.201700372 (22. 12. 2019).

  60. Ansari N., Lodha A., Pandya A., Sutariya P. G., Menon S. K. Lab-on-phone citrate-capped silver nanosensor for lidocaine hydrochloride detection from a biological matrix. Anal. Methods 2015; 7, 9084–9091. https://doi.org/10.1039/C5AY01977J (24. 1. 2020).

  61. Jafari M., Tashkhourian J., Absalan G. Chiral recognition of tryptophan enantiomers using chitosan-capped silver nanoparticles: Scanometry and spectrophotometry approaches. Talanta 2018; 178, 870–878. https://doi.org/10.1016/j.talanta.2017.10.005 (22. 12. 2019).

  62. Peng J., Ling J., Zhang X. Q., Zhang L. Y., Cao Q. E., Ding Z. T. A rapid, sensitive and selective colorimetric method for detection of ascorbic acid. Sens. Actuators B: Chem. 2015; 221, 708–716. https://doi.org/10.1016/j.snb.2015.07.002 (22. 12. 2019).

  63. Manmana Y., Chutvirasakul B., Suntornsuk L., Nuchtavorn N. Cost effective paper-based colorimetric devices for a simple assay of dopamine in pharmaceutical formulations using 3,3´,5,5´-tetramethylbenzidine-silver nitrate as a chromogenic reagent. Pharm. Sci. Asia 2019; 46, 270–277. doi:10.29090/psa.2019.04.018.0037 (26. 1. 2020).

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  65. Phadungcharoen N., Patrojanasophon P., Opanasopit P., Ngawhirunpat T., Chinsriwongkul A., Rojanarata T. Smartphone-based Ellman’s colourimetric methods for the analysis of d-penicillamine formulation and thiolated polymer. Int. J. Pharm. 2019; 558, 120–127. https://doi.org/10.1016/j.ijpharm.2018.12.078 (22. 12. 2019).

  66. Jornet-Martínez N., Samper-Avilés M., Herráez-Hernández, R., Campíns-Falcó P. Modifying the reactivity of copper (II) by its encapsulation into polydimethylsiloxane: A selective sensor for ephedrine-like compounds. Talanta 2019; 196, 300–308. https://doi.org/10.1016/j.talanta.2018.12.054 (22. 12. 2019).

  67. Solana-Altabella A., Sánchez-Iranzo M. H., Bueso-Bordils J. I., Lahuerta-Zamora L., Mellado-Romero A. M. Computer vision-based analytical chemistry applied to determining iron in commercial pharmaceutical formulations. Talanta 2018; 188, 349–355. https://doi.org/10.1016/j.talanta.2018.06.008 (22. 12. 2019).

  68. da Silva R. S., Borges E. M. Quantitative analysis using a flatbed scanner: aspirin quantification in pharmaceutical tablets. J. Chem. Educ. 2019; 96, 1519–1526. https://doi.org/10.1021/acs.jchemed.8b00620 (31. 1. 2020).

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70. Chaplenko A. A., Monogarova O. V., Oskolok K. V., Chaplenko S. A. Colorimetric and indirect X-ray fluorescence determination of drug substances using chemically modified polyurethane-foam absorbents. Pharm. Chem. J. 2017; 51, 726–730. https://doi.org/10.1007/s11094-017-1682-4 (22. 12. 2019).

  71. Oskolok K. V., Monogarova O. V., Chaplenko A. A. Colorimetry and indirect X-ray fluorescence determination of active ingredients in tetracycline hydrochloride drug and injection solution of B₁₂ vitamin using of polyurethane foam sorbents. Iraqi J. Pharm. Sci. 2017; 26, 7–11. https://www.iasj.net/iasj? func=fulltext&aId=135241 (2. 2. 2020).

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  74. Leng Y., Hu F., Ma C., Du C., Ma L., Xu J., Lin Q., Sang Z., Lu Z. Simple, rapid, sensitive, selective and label-free lincomycin detection by using HAuCl₄ and NaOH. RSC Adv. 2019; 9, 28248–28252. https://doi.org/10.1039/C9RA04095A (6. 2. 2020).

  75. Mohamed A. A., Mahmoud E. H., Khalil M. M. Development of a selective and sensitive colour reagent for gold and silver ions and its application to desktop scanner analysis. RSC Adv. 2019; 9, 36358–36365. https://doi.org/10.1039/C9RA06840F (3. 2. 2020).

  76. Gorbunova M. O., Shevchenko A. V., Apyari V. V., Furletov A. A., Volkov P. A., Garshev A. V., Dmitrienko S. G. Selective determination of chloride ions using silver triangular nanoplates and dynamic gas extraction. Sens. Actuators B: Chem. 2018; 256, 699–705. https://doi.org/10.1016/j.snb.2017.09.212 (22. 12. 2019).

  77. Gorbunova M. O., Bayan E. M. A novel paper-based sensor for determination of halogens and halides by dynamic gas extraction. Talanta 2019; 199, 513–521. https://doi.org/10.1016/j.talanta.2019.02.093 (22. 12. 2019).

  78. Gorbunova M. O., Baulina A. A., Kulyaginova M. S., Apyari V. V., Furletov A. A., Garshev A. V., Dmitrienko S. G. Determination of iodide based on dynamic gas extraction and colorimetric detection by paper modified with silver triangular nanoplates. Microchem. J. 2019; 145, 729–736. https://doi.org/10.1016/j.microc.2018.11.046 (22. 12. 2019).

  79. Gorbunova M. O., Baulina A. A., Kulyaginova M. S., Apyari V. V., Furletov A. A., Volkov P. A., Bochenkov V. E., Starukhin A. S., Dmitrienko S. G. Dynamic gas extraction of iodine in combination with a silver triangular nanoplate-modified paper strip for colorimetric determination of iodine and of iodine-interacting compounds. Microchim. Acta 2019; 186, 188. https://doi.org/10.1007/s00604-019-3300-5 (22. 12. 2019).

  80. Chaplenko A. A., Monogarova O. V., Oskolok K. V Spectroscopic and colorimetric determination of meloxicam, lornoxicam, tenoxicam in drugs. IJPBA 2018; 9, 31–35. Available Online at www.ijpba.info (8. 2. 2020).

  81. Bridgeman D., Corral J., Quach A., Xian X., Forzani E. Colorimetric humidity sensor based on liquid composite materials for the monitoring of food and pharmaceuticals. Langmuir 2014; 30, 10785–10791. https://doi.org/10.1021/la502593g (8. 2. 2020).

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84. Fakayode O. J., Songca S. P., Oluwafemi O. S. Application of iron (III) meso-tetrakis (4-hydroxyphenyl) porphyrin-methylene blue strips for the detection and quantification of H₂O₂ in aqueous and pharmaceutical fluids. MRS Commun. 2019; 9, 398–405. htps://doi.org/10.1557/mrc.2019.14 (19. 12. 2019).

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