In-line derivative spectroscopy as a promising application to a small-scale in vitro transfer model in biorelevant supersaturation and precipitation testing

被引:14
作者
Jede, Christian [1 ,2 ]
Wagner, Christian [2 ]
Kubas, Holger [2 ]
Weber, Christian [3 ]
Weitschies, Werner [1 ]
机构
[1] Ernst Moritz Arndt Univ Greifswald, Inst Pharm, Dept Biopharmaceut & Pharmaceut Technol, Felix Hausdorff Str 3, D-17489 Greifswald, Germany
[2] Merck KGaA, Dept Pharmaceut Technol Chem & Pharmaceut Dev, Darmstadt, Germany
[3] Merck KGaA, Chem & Pharmaceut Dev, Darmstadt, Germany
关键词
biorelevant; derivative spectroscopy; dissolution; in-line analytics; supersaturation; precipitation; transfer model; DISSOLUTION RATE; SOLUBLE DRUGS; WEAK BASE; CARBAMAZEPINE; SOLUBILITY; ABSORPTION; PREDICTION; MEDIA; WATER;
D O I
10.1111/jphp.12991
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
ObjectivesDissolution testing of poorly soluble and precipitating drugs is of great importance for pharmaceutical industry. As offline HPLC analytics is time-consuming and labour-intensive, the development of suitable in-line analytics to measure drug concentration allows better predictions of drug dissolution and precipitation. The purpose of this study was to develop an in-line derivative spectroscopic method which facilitates drug concentration measurements in suspensions without additional sample preparation. MethodsSolubility, dissolution and precipitation of ketoconazole were analysed using derivative spectroscopy and HPLC. Key findingsResults of solubility and dissolution experiments were highly comparable. Due to higher sampling frequency and lack of sample preparations, supersaturation in a pH-shift experiment was more accurately captured by UV in-line analytics. The application of a prefiltration step and flow-through cuvettes facilitates implementation of in-line derivative spectroscopy into an in vitro transfer model with changing UV-active media and high supersaturation in highly turbid samples. ConclusionsAlthough the application of derivative spectroscopy has been described previously, the approach described herein is novel and well-suited for the application in an automated in vitro transfer model. Moreover, it represents a promising tool for drug substance characterisation, candidate selection and formulation development.
引用
收藏
页码:1315 / 1323
页数:9
相关论文
共 25 条
[1]   Interlaboratory Validation of Small-Scale Solubility and Dissolution Measurements of Poorly Water-Soluble Drugs [J].
Andersson, Sara B. E. ;
Alvebratt, Caroline ;
Bevernage, Jan ;
Bonneau, Damien ;
Mathews, Claudia da Costa ;
Dattani, Rikesh ;
Edueng, Khadijah ;
He, Yan ;
Holm, Rene ;
Madsen, Cecilie ;
Mueller, Thomas ;
Muenster, Uwe ;
Mullertz, Anette ;
Ojala, Krista ;
Rades, Thomas ;
Sieger, Peter ;
Bergstrom, Christel A. S. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2016, 105 (09) :2864-2872
[2]  
[Anonymous], 2018, USP40 NF35 GEN CHAPT
[3]   Technical note:: Miniaturized intrinsic dissolution rate (Mini-IDR™) measurement of griseofulvin and carbamazepine [J].
Berger, Cynthia M. ;
Tsinman, Oksana ;
Voloboy, Dmytro ;
Lipp, Dana ;
Stones, Steven ;
Avdeef, Alex .
DISSOLUTION TECHNOLOGIES, 2007, 14 (04) :39-41
[4]   Prediction of oral absorption of cinnarizine - A highly supersaturating poorly soluble weak base with borderline permeability [J].
Berlin, Mark ;
Przyklenk, Karl-Heinz ;
Richtberg, Annette ;
Baumann, Wolfgang ;
Dressman, Jennifer B. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2014, 88 (03) :795-806
[5]   Monitoring ibuprofen release from multiparticulates: In situ fiber-optic technique versus the HPLC method: A technical note [J].
Bijlani, Vishal ;
Yuonayel, Domotiere ;
Katpally, Sabitha ;
Chukwumezie, Beatrice Nkem ;
Adeyeye, Moji Christianah .
AAPS PHARMSCITECH, 2007, 8 (03)
[6]  
Bynum K., 2001, DISSOLUT TECHNOL, V8, P13
[7]   PHARMACEUTICAL APPLICATIONS OF SOLID DISPERSION SYSTEMS [J].
CHIOU, WL ;
RIEGELMAN, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1971, 60 (09) :1281-+
[8]   Mechanism-based selection of stabilization strategy for amorphous formulations: Insights into crystallization pathways [J].
Edueng, Khadijah ;
Mahlin, Denny ;
Larsson, Per ;
Bergstrom, Christel A. S. .
JOURNAL OF CONTROLLED RELEASE, 2017, 256 :193-202
[9]   Dissolution Rate and Apparent Solubility of Poorly Soluble Drugs in Biorelevant Dissolution Media [J].
Fagerberg, Jonas H. ;
Tsinman, Oksana ;
Sun, Na ;
Tsinman, Konstantin ;
Avdeef, Alex ;
Bergstrom, Christel A. S. .
MOLECULAR PHARMACEUTICS, 2010, 7 (05) :1419-1430
[10]   High-throughput drug discovery: what can we exulect from HTS? [J].
Gribbon, P ;
Sewing, A .
DRUG DISCOVERY TODAY, 2005, 10 (01) :17-22