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Items: 1 to 20 of 105

1.

The formation of furfural compounds in selected saccharide- and polysaccharide-based pharmaceutical excipients.

Douša M, Gibala P, Břicháč J, Havlíček J.

J Pharm Sci. 2012 May;101(5):1811-20. doi: 10.1002/jps.23072. Epub 2012 Feb 8.

PMID:
22318787
2.

Drug-excipient compatibility testing-Identification and characterization of degradation products of phenylephrine in several pharmaceutical formulations against the common cold.

Douša M, Gibala P, Havlíček J, Plaček L, Tkadlecová M, Břicháč J.

J Pharm Biomed Anal. 2011 Jul 15;55(5):949-56. doi: 10.1016/j.jpba.2011.03.027. Epub 2011 Mar 25.

PMID:
21481557
3.

A multidisciplinary approach to identify a degradation product in a pharmaceutical dosage form.

Pan C, Guan J, Lin M.

J Pharm Biomed Anal. 2011 Mar 25;54(4):855-9. doi: 10.1016/j.jpba.2010.10.016. Epub 2010 Oct 27.

PMID:
21129882
6.

Kinetics and mechanism of the hydrolysis of thiamethoxam.

Karmakar R, Singh SB, Kulshrestha G.

J Environ Sci Health B. 2009 Jun;44(5):435-41. doi: 10.1080/03601230902934785.

PMID:
20183047
7.

Degradation kinetics and mechanism of an oxadiazole derivative, design of a stable drug product for BMS-708163, a γ-secretase inhibitor drug candidate.

Hartley RF, Huang Y, Cassidy M, Razler TM, Qian F, Hussain MA.

J Pharm Sci. 2012 Sep;101(9):3124-33. doi: 10.1002/jps.23050. Epub 2012 Jan 19.

PMID:
22262489
8.

Critical practical aspects in the application of liquid chromatography-mass spectrometric studies for the characterization of impurities and degradation products.

Narayanam M, Handa T, Sharma P, Jhajra S, Muthe PK, Dappili PK, Shah RP, Singh S.

J Pharm Biomed Anal. 2014 Jan;87:191-217. doi: 10.1016/j.jpba.2013.04.027. Epub 2013 Apr 28. Review.

PMID:
23706957
9.

Structure elucidation and quantification of impurities formed between 6-aminocaproic acid and the excipients citric acid and sorbitol in an oral solution using high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy.

Schou-Pedersen AM, Cornett C, Nyberg N, Østergaard J, Hansen SH.

J Pharm Biomed Anal. 2015 Mar 25;107:333-40. doi: 10.1016/j.jpba.2015.01.022. Epub 2015 Jan 19.

PMID:
25645337
10.

Forced degradation and impurity profiling: recent trends in analytical perspectives.

Jain D, Basniwal PK.

J Pharm Biomed Anal. 2013 Dec;86:11-35. doi: 10.1016/j.jpba.2013.07.013. Epub 2013 Jul 31. Review.

PMID:
23969330
11.

Quantitation of acetol in common pharmaceutical excipients using LC-MS.

Beilin E, Baker LJ, Culbert P, Toltl NP.

J Pharm Biomed Anal. 2008 Jan 22;46(2):316-21. Epub 2007 Oct 23.

PMID:
18054457
12.

Screening of synthetic PDE-5 inhibitors and their analogues as adulterants: analytical techniques and challenges.

Patel DN, Li L, Kee CL, Ge X, Low MY, Koh HL.

J Pharm Biomed Anal. 2014 Jan;87:176-90. doi: 10.1016/j.jpba.2013.04.037. Epub 2013 May 6. Review.

PMID:
23721687
13.

5-hydroxymethyl-2-furfural and derivatives formed during acid hydrolysis of conjugated and bound phenolics in plant foods and the effects on phenolic content and antioxidant capacity.

Chen PX, Tang Y, Zhang B, Liu R, Marcone MF, Li X, Tsao R.

J Agric Food Chem. 2014 May 21;62(20):4754-61. doi: 10.1021/jf500518r. Epub 2014 May 12.

PMID:
24796380
14.

Influence of formaldehyde impurity in polysorbate 80 and PEG-300 on the stability of a parenteral formulation of BMS-204352: identification and control of the degradation product.

Nassar MN, Nesarikar VN, Lozano R, Parker WL, Huang Y, Palaniswamy V, Xu W, Khaselev N.

Pharm Dev Technol. 2004;9(2):189-95.

PMID:
15202578
15.

Identification of imatinib mesylate degradation products obtained under stress conditions.

Szczepek WJ, Kosmacińska B, Bielejewska A, Łuniewski W, Skarzyński M, Rozmarynowska D.

J Pharm Biomed Anal. 2007 Apr 11;43(5):1682-91. Epub 2007 Jan 12.

PMID:
17307328
16.

Identification of reaction products between drug substances and excipients by HPLC-SPE-NMR: ester and amide formation between citric acid and 5-aminosalicylic acid.

Larsen J, Staerk D, Cornett C, Hansen SH, Jaroszewski JW.

J Pharm Biomed Anal. 2009 Apr 5;49(3):839-42. doi: 10.1016/j.jpba.2008.12.028. Epub 2008 Dec 27.

PMID:
19185440
17.

On-line coupling of size exclusion chromatography with mixed-mode liquid chromatography for comprehensive profiling of biopharmaceutical drug product.

He Y, Friese OV, Schlittler MR, Wang Q, Yang X, Bass LA, Jones MT.

J Chromatogr A. 2012 Nov 2;1262:122-9. doi: 10.1016/j.chroma.2012.09.012. Epub 2012 Sep 10.

PMID:
22999205
18.

Hydrolysis of sorghum straw using phosphoric acid: evaluation of furfural production.

Vázquez M, Oliva M, Téllez-Luis SJ, Ramírez JA.

Bioresour Technol. 2007 Nov;98(16):3053-60. Epub 2006 Dec 4.

PMID:
17145181
19.

The use of mixed-mode ion-exchange solid phase extraction to characterize pharmaceutical drug degradation.

Landis MS.

J Pharm Biomed Anal. 2007 Sep 3;44(5):1029-39. Epub 2007 Apr 29.

PMID:
17553650
20.

Analysis of aldehydes in excipients used in liquid/semi-solid formulations by gas chromatography-negative chemical ionization mass spectrometry.

Li Z, Kozlowski BM, Chang EP.

J Chromatogr A. 2007 Aug 10;1160(1-2):299-305. Epub 2007 Jun 7.

PMID:
17586516
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