Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
Más filtros










Intervalo de año de publicación
1.
Int J Pharm ; 643: 123259, 2023 Aug 25.
Artículo en Inglés | MEDLINE | ID: mdl-37479100

RESUMEN

The incidences of antimicrobial resistance in particular, Methicillin-Resistant Staphylococcus aureus (MRSA) have increased during the last two decades. However, conventional dosage forms are unable to evade the barrier effect of the stratum corneum to permit deep penetration of the skin to resolve deep skin infections. There is, therefore, an urgent need for an advanced drug delivery system. Thus the study reported herein was aimed to fabricate a novasome-loaded luteolin (LUT) to improve its topical delivery and to enhance its antibacterial activity. The system was investigated for the impact of the type of surfactant, stearic acid concentration (g %), cholesterol amount (mg) and Brij 52 amount (mg) on the percent entrapment efficiency, particle size, poly-dispersity index and zeta potential. Statistical optimization of these factors was conducted using the Design-Expert® software. The optimum formulation was further in-vitro characterized by release study, differential scanning calorimetry, transmission electron microscope, x-ray diffraction and antibacterial activity. Formulation F2 composed of Span 60, 0.4 g % of stearic acid, 100 mg cholesterol and 30 mg Brij 52 was selected as the optimum formula based on the highest desirability value (0.634). F2 demonstrated enhanced antimicrobial activity with lower minimum inhibitory concentrations against a panel of MRSA clinical isolates when compared to LUT dispersion. Furthermore, the F2 formula exhibited higher anti-virulence activity by effectively inhibiting biofilm formation and suppressing α-hemolysin activity in MRSA isolates. It also demonstrated improved biosafety based on cytotoxicity assessment on human skin fibroblasts (HSF). Finally, when assessed in an in vivo skin infection mouse model, the F2 formula and commercially available fusidic acid preparation significantly reduced the microbial load of infected skin lesions compared to both the negative control and LUT dispersion-treated groups. Based on the aforementioned results, the validity of novasomes as a nano-carrier to boost in vitro and in vivo anti-MRSA activity of LUT could be affirmed.


Asunto(s)
Staphylococcus aureus Resistente a Meticilina , Infecciones Estafilocócicas , Humanos , Animales , Ratones , Ácidos Grasos no Esterificados , Luteolina/farmacología , Luteolina/uso terapéutico , Cetomacrogol/farmacología , Cetomacrogol/uso terapéutico , Antibacterianos , Pruebas de Sensibilidad Microbiana , Infecciones Estafilocócicas/tratamiento farmacológico , Infecciones Estafilocócicas/microbiología
2.
Antiviral Res ; 158: 238-243, 2018 10.
Artículo en Inglés | MEDLINE | ID: mdl-30153444

RESUMEN

Condylomata acuminata (CA) or anogenital warts are benign proliferative lesions caused by low-risk human papillomaviruses (HPV). Treating CA can be very frustrating for patients and clinicians due to the high recurrence rates. Immunosuppression is associated with larger size of CA that are more frequently resistant to treatment. Surgical approaches tend to be poorly effective in the long-term because of high recurrence rates related to the persistence of HPV-infected cells. In our search to find an agent to treat intraurethral CA with minor or no side effects, we evaluated intraurethral cidofovir in two male patients, who were under immunosuppressing therapy due to organ transplantation and suffered from extensive urethral HPV lesions. Both patients underwent biopsy of the lesions and initial transurethral resection. In our first case, intraurethral cidofovir instillations were started after 2 months due to recurrence after surgical treatment. In our second case, intraurethral cidofovir was administered after surgery because of incomplete resection of extensive lesions. Because of persistent or rapidly recurrent lesions despite intraurethral cidofovir instillations, the first patient needed two additional surgical interventions while the second patient underwent one additional surgical intervention. After surgical intervention, both patients received again adjuvant cidofovir instillations without side effects. Over a period of 56 weeks, both patients received each a total of 28 instillations with cidofovir. Following 3.5 years (patient 1) of the last cidofovir instillation, no recurrences were observed in our first patient. Following 6 months of the last cidofovir instillation (patient 2), two very small recurrent lesions in the most distal part of the urethra were observed in our second patient for which he will receive a cycle of 6 cidofovir instillations in the near future. Intraurethral cidofovir is a safe, easy-to-use, well-tolerated and an effective adjuvant to surgery for extensive intraurethral CA in immunocompromised patients.


Asunto(s)
Cidofovir/uso terapéutico , Condiloma Acuminado/tratamiento farmacológico , Condiloma Acuminado/cirugía , Huésped Inmunocomprometido , Papillomaviridae/efectos de los fármacos , Infecciones por Papillomavirus/tratamiento farmacológico , Administración Tópica , Adulto , Biopsia , Cetomacrogol/uso terapéutico , Condiloma Acuminado/patología , Humanos , Terapia por Láser , Masculino , Persona de Mediana Edad , Trasplante de Órganos , Infecciones por Papillomavirus/virología , Recurrencia
3.
Clin Dermatol ; 31(6): 787-91, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24160288

RESUMEN

There is now scientific evidence of genetically driven skin-barrier anomalies in atopic patients. These barrier anomalies facilitate sustained antigen ingress through the defective barrier, which can bring about a Th2-dominant response. It enhances the transepidermal water loss, resulting in dry skin and leading to the release of preformed proinflammatory cytokines and to a cascade of events ending up in inflammation.


Asunto(s)
Dermatitis Atópica/tratamiento farmacológico , Dermatitis Atópica/fisiopatología , Emolientes/uso terapéutico , Crema para la Piel/uso terapéutico , Pérdida Insensible de Agua , Amidas , Ceramidas/uso terapéutico , Cetomacrogol/uso terapéutico , Colesterol/uso terapéutico , Dermatitis Atópica/inmunología , Combinación de Medicamentos , Endocannabinoides/uso terapéutico , Etanolaminas/uso terapéutico , Ácidos Grasos/uso terapéutico , Alcoholes Grasos/uso terapéutico , Humanos , Aceite Mineral/uso terapéutico , Medicamentos sin Prescripción/uso terapéutico , Ácidos Palmíticos/uso terapéutico , Vaselina/uso terapéutico , Medicamentos bajo Prescripción/uso terapéutico
5.
J Adv Nurs ; 16(8): 952-6, 1991 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-1779084

RESUMEN

A double-blind clinical trial was conducted to compare the efficacy of an active based cream against a placebo non-active based cream in the healing of superficial pressure ulcers in a population of geriatric hospital patients and residents in community nursing homes. The active group showed a small significant beneficial effect at week four. The overall results of the trial also demonstrated a significant improvement in ulcer size over the duration of the trial period in both active and placebo groups.


Asunto(s)
Cetomacrogol/uso terapéutico , Hordeum , Extractos Vegetales/uso terapéutico , Úlcera por Presión/tratamiento farmacológico , Administración Tópica , Anciano , Anciano de 80 o más Años , Cetomacrogol/administración & dosificación , Método Doble Ciego , Combinación de Medicamentos , Femenino , Humanos , Masculino , Evaluación en Enfermería , Placebos , Extractos Vegetales/administración & dosificación , Extractos Vegetales/farmacología , Úlcera por Presión/epidemiología , Úlcera por Presión/enfermería , Factores de Riesgo , Cicatrización de Heridas/efectos de los fármacos
6.
J Adv Nurs ; 3(4): 373-82, 1978 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-248384

RESUMEN

A preliminary trial was carried out to establish the most suitable hygienic wipe for sanitary cleansing in incontinence and to study and compare the difference between cleansing with soap and non-ionic detergents in incontinent patients. Four non-ionic detergents were tested against National Health toilet soap in 290 incontinent episodes. Other observations were made on the skin condition following cleansing, the ease of cleansing, odour control, detergency, and allergenicity. The results showed that a scrim wipe was the best for this purpose and also indicated that the non-ionic detergent Cetomacrogol 1000 B.P.C. to be preferential to all other creams and soap in the time taken for cleansing. The skin condition, odour control and detergent ability were all superior with this cream. It was revealed by the trial that in cleansing faecal incontinence with non-ionic detergent, an initial wipe, followed by about 7.0 grams of detergent on a moistened wipe to achieve emulsification and than followed by another dry wipe, is all that is required. The condition of the skin was recorded as excellent and the figures indicated a possible saving of 20% in nursing time.


Asunto(s)
Cetomacrogol/uso terapéutico , Incontinencia Fecal/enfermería , Higiene , Polietilenglicoles/uso terapéutico , Cetomacrogol/farmacología , Humanos , Iones , Enfermedades de la Piel/prevención & control , Jabones/farmacología , Jabones/uso terapéutico
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA