Mass independence and asymmetry of the reaction: Multi-fragmentation as an example

We present our recent results on the fragmentation by varying the mass asymmetry of the reaction between 0.2 and 0.7 at an incident energy of 250 MeV/nucleon. For the present study, the total mass of the system is kept constant (ATOT = 152) and mass asymmetry of the reaction is defined by the asymmetry parameter (? = | (AT - AP)/(AT + AP) |). The measured distributions are shown as a function of the total charge of all projectile fragments, Zbound. We see an interesting outcome for rise and fall in the production of intermediate mass fragments (IMFs) for large asymmetric colliding nuclei. This trend, however, is completely missing for large asymmetric nuclei. Therefore, experiments are needed to verify this prediction

Isospin effects on the energy of vanishing flow in heavy-ion collisions

Using the isospin-dependent quantum molecular dynamics model we study the isospin effects on the disappearance of flow for the reactions of $^{58}Ni$ + $^{58}Ni$ and $^{58}Fe$ +$^{58}Fe$ as a function of impact parameter. We found good agreement between our calculations and experimentally measured energy of vanishing flow at all colliding geometries. Our calculations reproduce the experimental data within 5%(10%) at central (peripheral) geometries

A comparative study of model ingredients: fragmentation in heavy-ion collisions using quantum molecular dynamics model

We aim to understand the role of NN cross-sections, equation of state as well as different model ingredients such as width of Gaussian, clusterisation range and different clusterisation algorithms in multifragmentation using quantum molecular dynamics model. We notice that all model ingredients have sizable effect on the fragment pattern.Comment: 12 Pages, 4 Figure

Komprimirani matriksni dvokomponentni sustavi s metoklopramid hidrokloridom

The purpose of the present investigation was to produce a quick/slow biphasic delivery system for metoclopramide hydrochloride using the superdisintegrant Ac-di-sol for the fast release layer and hydroxypropyl methylcellulose K100M and Ucarflock 302 to modulate the release of the drug. A dual component tablet made up of a sustained release and an immediate release layer was prepared by direct compression. A 32 full factorial design was applied to systematically optimize the drug release profile of the sustained release layer. The results of the full factorial design indicate that a small amount of HPMC K100M and a large amount of Ucarflock 302 favor sustained release of the metoclopramide hydrochloride vaginal dual component system. The ex vivo residence time reveals that the formulation was retained for more than 10 h. The formulation gave an initial burst effect to provide the loading dose of the drug followed by sustained release for 12 h, thus solving the problem of repeated administration, especially in pregnancy.Cilj rada bila je priprava brzog/sporog bifazičnog sustava za isporuku metoklopramid hidroklorida koristeći dezintegrator Ac-di-sol za sloj koji brzo oslobađa i hidroksipropil metilcelulozu K100M i Ucarflock 302 za moduliranje oslobađanja ljekovite tvari. Dvokomponentna tableta sa slojem za usporeno i slojem za brzo oslobađanje pripravljena je metodom izravne kompresije. 32 faktorijalni dizajn primijenjen je za sistematsko optimiranje profila oslobađanja ljekovite tvari u sloju za usporeno oslobađanje. Rezultati ukazuju na to da su mala količina HPMC K100M i velika količina Ucarflock 302 bitne za usporeno oslobađanje metoklopramid hidroklorida u dvokomponentnom sustavu za vaginalnu upotrebu. Ex vivo ispitivanja pokazuju da se pripravak zadržava više od 10 h. Naglo oslobađanje lijeka omogućava brzo postizanje udarne doze, a postupno oslobađanje tijekom 12 h održavanje učinkovite koncentracije, čime se rješava problem opetovane primjene, posebno u trudnoći

Model and experiences of initiating collaboration with traditional healers in validation of ethnomedicines for HIV/AIDS in Namibia

Many people with Human Immunodeficiency Virus/Acquired Immunodeficiency Syndrome (HIV/AIDS) in Namibia have access to antiretroviral drugs but some still use traditional medicines to treat opportunistic infections and offset side-effects from antiretroviral medication. Namibia has a rich biodiversity of indigenous plants that could contain novel anti-HIV agents. However, such medicinal plants have not been identified and properly documented. Various ethnomedicines used to treat HIV/AIDS opportunistic infections have not been scientifically validated for safety and efficacy. These limitations are mostly attributable to the lack of collaboration between biomedical scientists and traditional healers. This paper presents a five-step contextual model for initiating collaboration with Namibian traditional healers in order that candidate plants that may contain novel anti-HIV agents are identified, and traditional medicines used to treat HIV/AIDS opportunistic infections are subjected to scientific validation. The model includes key structures and processes used to initiate collaboration with traditional healers in Namibia; namely, the National Biosciences Forum, a steering committee with the University of Namibia (UNAM) as the focal point, a study tour to Zambia and South Africa where other collaborative frameworks were examined, commemorations of the African Traditional Medicine Day (ATMD), and consultations with stakeholders in north-eastern Namibia. Experiences from these structures and processes are discussed. All traditional healers in north-eastern Namibia were willing to collaborate with UNAM in order that their traditional medicines could be subjected to scientific validation. The current study provides a framework for future collaboration with traditional healers and the selection of candidate anti-HIV medicinal plants and ethnomedicines for scientific testing in Namibia

Pregnancy-related pelvic girdle pain: an update

A large number of scientists from a wide range of medical and surgical disciplines have reported on the existence and characteristics of the clinical syndrome of pelvic girdle pain during or after pregnancy. This syndrome refers to a musculoskeletal type of persistent pain localised at the anterior and/or posterior aspect of the pelvic ring. The pain may radiate across the hip joint and the thigh bones. The symptoms may begin either during the first trimester of pregnancy, at labour or even during the postpartum period. The physiological processes characterising this clinical entity remain obscure. In this review, the definition and epidemiology, as well as a proposed diagnostic algorithm and treatment options, are presented. Ongoing research is desirable to establish clear management strategies that are based on the pathophysiologic mechanisms responsible for the escalation of the syndrome's symptoms to a fraction of the population of pregnant women

Spectator fragmentation in nucleus-nucleus collisions: Phase space approach

Dynamics of spectator matter break-up in non-central collisions of $^{197}$Au+ $^{197}$Au at 1000 AMeV are explored within framework of quantum molecular dynamics (QMD) model. The phase space of nucleons bound in intermediate mass fragments are studied using two clusterization subroutines. Backtracking the origin of fragments to the time of initial contact between colliding nuclei indicates that \textit{simulated annealing clusterization algorithm} (SACA) results into significant yield of projectile-like and target-like fragments. Simplest clusterization approach based on spatial correlation technique, however, predicted much lesser production probability of fragments in spectator zone.Comment: Abstract accepted in Rutherford Centennial Conference on Nuclear Physics 201