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1University of Ljubljana[Affiliation] Publications | LitMetric

10 results match your criteria: "1University of Ljubljana[Affiliation]"

Lipid-based systems, such as self-microemulsifying systems (SMEDDS) are attracting strong attention as a formulation approach to improve the bioavailability of poorly water-soluble drugs. By applying the "spring and parachute" strategy in designing supersaturable SMEDDS, it is possible to maintain the drug in the supersaturated state long enough to allow absorption of the complete dose, thus improving the drug's bio-availability. As such an approach allows the incorporation of larger amounts of the drug in equal or even lower volumes of SMEDDS, it also enables the production of smaller final dosage forms as well as decreased gastrointestinal irritation, being of particular importance when formulating dosage forms for children or the elderly.

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Article Synopsis
  • - Society is focusing on the need for innovative pharmaceutical technologies to address challenges like population aging and climate change, particularly targeting patient-specific drug delivery systems.
  • - The development of protein drugs for subcutaneous administration is crucial but faces challenges such as maintaining protein stability and appropriate formulation viscosity during manufacturing.
  • - A study using bovine serum albumin explored how protein concentration impacts the quality of liquid and lyophilized formulations, confirming that higher concentrations lead to increased viscosity and longer reconstitution times, while identifying the critical role of sucrose and the need to balance it with mannitol in lyophilization.
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The principal function of skin is to form an effective barrier between the human body and its environment. Impaired barrier function represents a precondition for the development of skin diseases such as atopic dermatitis (AD), which is the most common inflammatory skin disease characterized by skin barrier dysfunction. AD significantly affects patients' quality of life, thus, there is a growing interest in the development of novel delivery systems that would improve therapeutic outcomes.

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This study investigates the 10-year trend in the sedative and anticholinergic burden among older adults in Slovenia, with the aim of identifying opportunities to optimize pharmacotherapy in this population. A retrospective drug utilization analysis was conducted based on a national anonymized database of dispensed prescriptions from 2009 to 2019. The study employed the sedative load model and the anticholinergic cognitive burden scale to assess the sedative and anti cholinergic burden, respectively.

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Deprescribing: An umbrella review.

Acta Pharm

June 2024

1University of Ljubljana Faculty of Pharmacy, Department of Social Pharmacy 1000 Ljubljana, Slovenia.

This umbrella review examined systematic reviews of deprescribing studies by characteristics of intervention, population, medicine, and setting. Clinical and humanistic outcomes, barriers and facilitators, and tools for deprescribing are presented. The Medline database was used.

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Article Synopsis
  • In chronic heart failure (CHF) patients, angiotensin-converting enzyme inhibitors like ramipril are recommended to help prevent worsening conditions and reduce hospitalizations.
  • A study involving 23 CHF patients examined how body composition affects the pharmacokinetics of ramipril and its active form, ramiprilat, over time.
  • Findings indicated that ramipril clearance is influenced by patient age and dosage, while ramiprilat clearance is related to kidney function and dosage; however, pharmacokinetics remained stable over the study period, suggesting biennial outpatient evaluations are sufficient for monitoring therapy.
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Forecasting the effect of water gastric emptying patterns on model drug release in an glass-bead flow-through system.

Acta Pharm

June 2024

1University of Ljubljana, Faculty of Pharmacy Department of Biopharmaceutics and Pharmacokinetics 1000 Ljubljana, Slovenia.

Oral solid dosage forms are most frequently administered with a glass of water which empties from the stomach relatively fast, but with a certain variability in its emptying kinetics. The purpose of this study was thus to simulate different individual water gastric emptying (GE) patterns in an glass-bead flow-through dissolution system. Further, the effect of GE on the dissolution of model drugs from immediate-release tablets was assessed by determining the amount of dissolved drug in the samples pumped out of the stomach compartment.

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Remifentanil is an ultra-short-acting synthetic opioid-class analgesic which might be increasingly used "off-label" as pain management during labour. Side effects in parturients during labour, and in the infant at birth are of particular concern, especially respiratory depression which is concentration-dependent, and can occur at levels as low as 3-5 ng mL. The safety of such use, particularly in newborns due to remifentanil placental transfer, has not been fully demonstrated yet, partly due to the lack of a suitable non-invasive analytical method.

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The aim of this study was to externally validate the predictive performance of published population pharmacokinetic models of gentamicin in all paediatric age groups, from preterm newborns to adolescents. We first selected published population pharmacokinetic models of gentamicin developed in the paediatric population with a wide age range. The parameters of the literature models were then re-estimated using the PRIOR subroutine in NONMEM.

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The aim of this study was to evaluate the efficacy and safety of electrochemotherapy (ECT) with bleomycin for treatment of squamous cell carcinoma (SCC) in cats. Between March 2008 and October 2011, 11 cats with 17 superficial SCC nodules in different clinical stages (ranging from Tis to T4), located on nasal planum (6/11), pinnae (3/11) and both locations (2/11), were included in a prospective non-randomised study. Sixteen of 17 SCC nodules were treated with ECT (15/16 with single session and in one case with two sessions); one nodule was surgically removed.

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