2.5
Impact Factor
4.6
CiteScore
23 days
Time to First Decision

Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2016). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).

Scientia Pharmaceutica, Volume 79, Issue 2

June 2011 - 13 articles

Issues are regarded as officially published after their release is announced to the table of contents alert mailing list .
You may sign up for email alerts to receive table of contents of newly released issues.
PDF is the official format for papers published in both, html and pdf forms. To view the papers in pdf format, click on the "PDF Full-text" link, and use the free Adobe Reader to open them.

Articles (13)

Select all

Article

6 Citations

1,831 Views

14 Pages

Synthesis and Biological Evaluation of New 3-Phenyl-1-[(4-arylpiperazin-1-yl)alkyl]- piperidine-2,6-diones

Anna BIELENICA,
Jerzy KOSSAKOWSKI,
Marta STRUGA,
Izabela DYBAŁA,
Roberta LODDO,
Cristina IBBA and
Paolo LA COLLA

Sci. Pharm.2011, 79(2), 225-238;https://doi.org/10.3797/scipharm.1012-17

12 February 2011

A set of 13 alkyl derivatives of 3-phenylpiperidine-2,6-dione were synthesized. Newly obtained compounds were investigated in vitro against HIV-1 and other selected viruses. The benzyl 3f and fluorophenyl 3g derivatives showed moderate protection aga...

Full Article

Article

20 Citations

2,572 Views

15 Pages

A New Validated Liquid Chromatographic Method for the Determination of Loratadine and its Impurities

Gajjela RAMULU,
Yalavarthi RAVINDRA KUMAR,
Krishnamurthy VYAS,
Mulukutla V. SURYANARAYANA and
Khagga MUKKANTI

Sci. Pharm.2011, 79(2), 277-292;https://doi.org/10.3797/scipharm.1012-13

12 February 2011

An improved gradient, reversed-phase liquid chromatographic (RP-LC) method was developed and subsequently validated for the determination of Loratadine and its impurities/degradation products in pharmaceutical drug substance. Separation was achieved...

Full Article

Article

7 Citations

2,902 Views

14 Pages

A Validated Stability-Indicating Liquid-Chromatographic Method for Ranitidine Hydrochloride in Liquid Oral Dosage Form

Nitish SHARMA,
Surendra Singh RAO,
Pingili Sunil REDDY and
Annarapu MALLESWARA REDDY

Sci. Pharm.2011, 79(2), 309-322;https://doi.org/10.3797/scipharm.1101-06

12 February 2011

A selective, specific and stability-indicating gradient reverse phase highperformance liquid chromatographic (HPLC) method was developed for the determination of Ranitidine in presence of its impurities, forced degradation products and placebo substa...

Full Article

of 2

Get Alerted

Add your email address to receive forthcoming issues of this journal.

Sci. Pharm. - ISSN 2218-0532

Imprint

Download Flyer