Kalantzi L - Search Results

1

Canine intestinal contents vs. simulated media for the assessment of solubility of two weak bases in the human small intestinal contents.

Kalantzi L, Persson E, Polentarutti B, Abrahamsson B, Goumas K, Dressman JB, Reppas C. Kalantzi L, et al. Pharm Res. 2006 Jun;23(6):1373-81. doi: 10.1007/s11095-006-0207-8. Epub 2006 May 25. Pharm Res. 2006. PMID: 16715357

2

The delayed dissolution of paracetamol products in the canine fed stomach can be predicted in vitro but it does not affect the onset of plasma levels.

Kalantzi L, Polentarutti B, Albery T, Laitmer D, Abrahamsson B, Dressman J, Reppas C. Kalantzi L, et al. Int J Pharm. 2005 May 30;296(1-2):87-93. doi: 10.1016/j.ijpharm.2005.02.028. Epub 2005 Apr 7. Int J Pharm. 2005. PMID: 15885459

3

Characterization of the human upper gastrointestinal contents under conditions simulating bioavailability/bioequivalence studies.

Kalantzi L, Goumas K, Kalioras V, Abrahamsson B, Dressman JB, Reppas C. Kalantzi L, et al. Pharm Res. 2006 Jan;23(1):165-76. doi: 10.1007/s11095-005-8476-1. Epub 2006 Dec 1. Pharm Res. 2006. PMID: 16308672 Clinical Trial.

4

Estimation of intragastric solubility of drugs: in what medium?

Vertzoni M, Pastelli E, Psachoulias D, Kalantzi L, Reppas C. Vertzoni M, et al. Among authors: kalantzi l. Pharm Res. 2007 May;24(5):909-17. doi: 10.1007/s11095-006-9209-9. Epub 2007 Mar 20. Pharm Res. 2007. PMID: 17372688

5

In vitro methods can forecast the effects of intragastric residence on dosage form performance.

Kalantzi L, Page R, Nicolaides E, Digenis G, Reppas C. Kalantzi L, et al. Eur J Pharm Sci. 2008 Apr 23;33(4-5):445-51. doi: 10.1016/j.ejps.2008.01.014. Epub 2008 Feb 9. Eur J Pharm Sci. 2008. PMID: 18343098

6

Biowaiver monographs for immediate release solid oral dosage forms: acetaminophen (paracetamol).

Kalantzi L, Reppas C, Dressman JB, Amidon GL, Junginger HE, Midha KK, Shah VP, Stavchansky SA, Barends DM. Kalantzi L, et al. J Pharm Sci. 2006 Jan;95(1):4-14. doi: 10.1002/jps.20477. J Pharm Sci. 2006. PMID: 16307451 Free article.

7

A Novel Rheological Method to Assess Drug-Polymer Interactions Regarding Miscibility and Crystallization of Drug in Amorphous Solid Dispersions for Oral Drug Delivery.

Tsakiridou G, Reppas C, Kuentz M, Kalantzi L. Tsakiridou G, et al. Among authors: kalantzi l. Pharmaceutics. 2019 Nov 22;11(12):625. doi: 10.3390/pharmaceutics11120625. Pharmaceutics. 2019. PMID: 31766731 Free PMC article.

8

Application of the solubility parameter concept to assist with oral delivery of poorly water-soluble drugs - a PEARRL review.

Jankovic S, Tsakiridou G, Ditzinger F, Koehl NJ, Price DJ, Ilie AR, Kalantzi L, Kimpe K, Holm R, Nair A, Griffin B, Saal C, Kuentz M. Jankovic S, et al. Among authors: kalantzi l. J Pharm Pharmacol. 2019 Apr;71(4):441-463. doi: 10.1111/jphp.12948. Epub 2018 Jul 5. J Pharm Pharmacol. 2019. PMID: 29978475 Review.

9

Lipophilicity and hydrophobicity considerations in bio-enabling oral formulations approaches - a PEARRL review.

Ditzinger F, Price DJ, Ilie AR, Köhl NJ, Jankovic S, Tsakiridou G, Aleandri S, Kalantzi L, Holm R, Nair A, Saal C, Griffin B, Kuentz M. Ditzinger F, et al. Among authors: kalantzi l. J Pharm Pharmacol. 2019 Apr;71(4):464-482. doi: 10.1111/jphp.12984. Epub 2018 Aug 2. J Pharm Pharmacol. 2019. PMID: 30070363 Review.

10

Recent advances in oral pulsatile drug delivery.

Kalantzi LE, Karavas E, Koutris EX, Bikiaris DN. Kalantzi LE, et al. Recent Pat Drug Deliv Formul. 2009 Jan;3(1):49-63. doi: 10.2174/187221109787158337. Recent Pat Drug Deliv Formul. 2009. PMID: 19149729 Review.

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