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Pharmaceutics, Volume 4, Issue 4

December 2012 - 9 articles

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Articles (9)

  • Article
  • Open Access
39 Citations
9,252 Views
25 Pages

SNEDDS Containing Poorly Water Soluble Cinnarizine; Development and in Vitro Characterization of Dispersion, Digestion and Solubilization

  • Anne T. Larsen,
  • Anayo Ogbonna,
  • Ragheb Abu-Rmaileh,
  • Bertil Abrahamsson,
  • Jesper Østergaard and
  • Anette Müllertz

14 December 2012

Self-Nanoemulsifying Drug Delivery Systems (SNEDDSs) were developed using well-defined excipients with the objective of mimicking digested SNEDDSs without the use of enzymes and in vitro lipolysis models and thereby enabling studies of the morphology...

  • Review
  • Open Access
46 Citations
12,585 Views
34 Pages

13 December 2012

Post-marketing detection and surveillance of potential safety hazards are crucial tasks in pharmacovigilance. To uncover such safety risks, a wide set of techniques has been developed for spontaneous reporting data and, more recently, for longitudina...

  • Article
  • Open Access
53 Citations
9,659 Views
17 Pages

Composition Influence on Pulmonary Delivery of Rifampicin Liposomes

  • Maria Letizia Manca,
  • Chiara Sinico,
  • Anna Maria Maccioni,
  • Octavio Diez,
  • Anna Maria Fadda and
  • Maria Manconi

27 November 2012

The effects of lipid concentration and composition on the physicochemical properties, aerosol performance and in vitro toxicity activity of several rifampicin-loaded liposomes were investigated. To this purpose, six liposome formulations containing d...

  • Review
  • Open Access
37 Citations
9,948 Views
27 Pages

7 November 2012

Antivascular treatments can either be antiangiogenic or targeting established tumour vasculature. These treatments affect the tumour microvasculature and microenvironment but may not change clinical measures like tumour volume and growth. In research...

  • Article
  • Open Access
100 Citations
13,734 Views
12 Pages

26 October 2012

Orodispersible dosage forms are promising new approaches for drug delivery. They enable an easy application, as there is no need to drink high amounts of liquids or swallow large solid dosage forms. The aim of the study was to develop an orodispersib...

  • Review
  • Open Access
74 Citations
10,111 Views
20 Pages

Artificial Neural Networks in Evaluation and Optimization of Modified Release Solid Dosage Forms

  • Svetlana Ibrić,
  • Jelena Djuriš,
  • Jelena Parojčić and
  • Zorica Djurić

18 October 2012

Implementation of the Quality by Design (QbD) approach in pharmaceutical development has compelled researchers in the pharmaceutical industry to employ Design of Experiments (DoE) as a statistical tool, in product development. Among all DoE technique...

  • Article
  • Open Access
37 Citations
9,082 Views
14 Pages

Bioavailability of a Lipidic Formulation of Curcumin in Healthy Human Volunteers

  • Yogesh B. Pawar,
  • Bhushan Munjal,
  • Saurabh Arora,
  • Manoj Karwa,
  • Gunjan Kohli,
  • Jyoti K. Paliwal and
  • Arvind K. Bansal

Numerous publications have reported the significant pharmacodynamic activity of Curcumin (CRM) despite low or undetectable levels in plasma. The objective of the present study was to perform a detailed pharmacokinetic evaluation of CRM after the oral...

  • Communication
  • Open Access
8 Citations
7,527 Views
16 Pages

One “Quality by Design” approach is the focus on the variability of the properties of the active substance. This is crucially important for active substances that are obtained from natural resources such as herbal plant material and extracts. In this...

  • Article
  • Open Access
6 Citations
7,012 Views
7 Pages

Compaction Behavior of Isomalt after Roll Compaction

  • Julian Quodbach,
  • Johanna Mosig and
  • Peter Kleinebudde

27 September 2012

The suitability of the new isomalt grade galenIQ™ 801 for dry granulation and following tableting is evaluated in this study. Isomalt alone, as well as a blend of equal parts with dibasic calcium phosphate, is roll compacted and tableted. Parti...

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Pharmaceutics - ISSN 1999-4923Creative Common CC BY license