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1.
Recenti Prog Med ; 112(3): 219-224, 2021 03.
Artigo em Italiano | MEDLINE | ID: mdl-33687361

RESUMO

The pandemic period has generated major problems in the pharmacies of hospitals and local health care companies regarding the distribution of drugs to patients undergoing treatment with chronic drugs. This is because the patient, during the lockdown, was forced to leave the house and go several miles away to reach the place where the drug was dispensed. Moreover, very often, the place was placed in covid-19 hospitals, like the one in Perugia, and was also a risk for the patient himself. The logistical organization allows, in addition to the advantages of traceability, efficiency and savings, with the arrival of the drug at home, a very high patient compliance that also translates into greater security in a pandemic period. To the Usl Umbria 1 of Perugia (Italy) has been centralized the activity of warehouse for all the South area that includes three hospitals and four sanitary districts. Such warehouse, through computerized procedure, guarantees the direct distribution with sending of the medicines directly to the district of belonging of the patient. In this way the patient was not forced to make long and risky trips to continue their chronic therapies. Moreover, this logistic warehouse has also allowed to cope with the correct management of many medicinal specialties that have been used against the SARS-CoV-2 virus avoiding their temporary deficiency for patients already on therapy according to the normal therapeutic indications (anti-inflammatory, antiretroviral and immunomodulatory). This paper aims to demonstrate how logistical organization is of vital importance for a National Health System that has to face increasing costs, ensure the traceability of all processes and, last but not least, survive a worldwide pandemic period.


Assuntos
Tratamento Farmacológico da COVID-19 , Armazenamento de Medicamentos , Pandemias , Preparações Farmacêuticas/provisão & distribuição , SARS-CoV-2 , Anti-Infecciosos/provisão & distribuição , Anti-Infecciosos/uso terapêutico , Anti-Inflamatórios/provisão & distribuição , Anti-Inflamatórios/uso terapêutico , Anti-Hipertensivos/provisão & distribuição , Anti-Hipertensivos/uso terapêutico , Antineoplásicos/provisão & distribuição , Antineoplásicos/uso terapêutico , Antivirais/provisão & distribuição , Antivirais/uso terapêutico , Área Programática de Saúde , Custos de Medicamentos/estatística & dados numéricos , Reposicionamento de Medicamentos , Armazenamento de Medicamentos/estatística & dados numéricos , Humanos , Fatores Imunológicos/provisão & distribuição , Fatores Imunológicos/uso terapêutico , Itália , Organização e Administração , Preparações Farmacêuticas/economia , Serviço de Farmácia Hospitalar/organização & administração
2.
Int J Oncol ; 27(6): 1559-66, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16273212

RESUMO

There is a general agreement on the fact that the Laboratory on chip (Lab-on-a-chip) technology will enable laboratory testing to move from laboratories employing complex equipments into non-laboratory settings. In this respect, dielectrophoresis (DEP) is a very valuable approach to design and produce Lab-on-a-chip devices able to manipulate microparticles and cells. In this study, we report the application of DEP-based devices for facilitating programmable interactions between microspheres and target tumor cells. We used two Lab-on-a-chip devices, one (the SmartSlide) carrying 193 parallel electrodes and generating up to 50 cylinder-shaped DEP cages, the other (the DEP array) carrying 102,400 arrayed electrodes and generating more than 10,000 spherical DEP cages. We determined whether these devices can be used to levitate and move microspheres and cells in order to obtain a forced interaction between microspheres and target cells. The first major point of this manuscript is that the DEP-based SmartSlide can be used for transfection experiments in which microspheres and target cells are forced to share the same DEP cage, leading to efficient binding of the microspheres to target cells. The data obtained using the DEP array show that this system allows the sequential, software-controlled binding of individually and independently moved single microspheres to a single target tumor cell. To our knowledge, this is the first report on the possible use of a DEP-based Lab-on-a-chip device for guided multiple binding of singularly moved microspheres to a single tumor cell. This approach can be of interest in the field of drug discovery, delivery and diagnosis.


Assuntos
Técnicas de Laboratório Clínico/instrumentação , Eletroforese/instrumentação , Microesferas , Algoritmos , Ligação Competitiva , Separação Celular/instrumentação , Simulação por Computador , Computadores , Desenho de Equipamento/métodos , Humanos , Células K562 , Modelos Biológicos , Reprodutibilidade dos Testes
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