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1.
Arq. bras. oftalmol ; 78(3): 194-196, May-Jun/2015. graf
Article in English | LILACS | ID: lil-753023

ABSTRACT

ABSTRACT Bevacizumab, a monoclonal anti-vascular endothelial growth factor antibody, has been suggested as a potential healing therapeutic following glaucoma surgery. Here, we aimed to improve the bioavailability of bevacizumab when used as an adjunct therapy to non-penetrating deep sclerectomy (DS) by using a bevacizumab-methylcellulose mixture (BMM). Ten previously non-operated eyes in ten patients diagnosed with primary open angle glaucoma underwent DS with a subconjunctival injection of 0.3 ml of BMM (bevacizumab 3.75 mg incorporated into 4% methylcellulose) at the surgical site. Bevacizumab release was evaluated in vitro using size-exclusion high performance liquid chromatography (HPLC). Intraocular pressure (IOP), bleb morphology, corneal endothelial cell count (CECC), and complications were evaluated at 6 months after surgery. Using HPLC, bevacizumab was detected in BMM for up to 72 h. Moreover, all surgical blebs remained expanded with hyaline material during the first week. A significant IOP reduction (mean ± SD= -10.3 ± 5.4 mmHg, P<0.001) and diffuse blebs were observed at the final follow-up period. Although CECC was slightly reduced (-7.4%), no complications were observed. In conclusion, bevacizumab was released from BMM, and the use of this innovative mixture yielded good results following DS with no complications. Further studies are required to determine its efficacy prior to establishing BMM as an adjunct treatment for penetrating and non-penetrating glaucoma surgeries.


RESUMO O bevacizumabe (um agente anti-fator de crescimento endotelial vascular) tem sido sugerido como potencial modulador cicatricial na cirurgia do glaucoma. Este estudo objetivou melhorar a biodisponibilidade do bevacizumabe, investigando a viabilidade de uma nova mistura de bevacizumabe-metilcelulose (BMM) como terapia adjuvante para a esclerectomia profunda não-penetrante (DS). Dez olhos sem cirurgias prévias de 10 pacientes com glaucoma primário de ângulo aberto foram submetidos à DS associada à uma injeção subconjuntival de 0,3 ml da mistura de bevacizumabe-metilcelulose (bevacizumabe 3,75 mg incorporado em metilcelulose 4%) no sítio cirúrgico. A liberação de bevacizumabe foi avaliada in vitro através de cromatografia líquida de alta performance por exclusão de tamanho (HPLC). A pressão intraocular (PIO), a morfologia da ampola de filtração, a contagem de células endoteliais da córnea (CECC) e as complicações foram estudadas aos seis meses de seguimento. O bevacizumabe foi detectado a partir da mistura de bevacizumabe-metilcelulose por meio do HPLC até 72 horas. Além disso, todas as ampolas cirúrgicas permaneceram expandidas com material hialino durante a primeira semana. Uma redução significativa da pressão intraocular (média ± DP= -10,3 ± 5,4 mmHg, P<0,001) e ampolas difusas foram observadas ao final do período de seguimento. Embora a contagem de células endoteliais da córnea se mostrou discretamente diminuída (-7,4%), nenhuma complicação foi observada. Neste estudo, o bevacizumabe foi liberado da mistura de bevacizumabe-metilcelulose e o uso desta nova mistura se associou com bons resultados cirúrgicos e nenhuma complicação. Estudos futuros serão necessários para determinar sua eficácia, antes de se estabelecer a mistura de bevacizumabe-metilcelulose como um tratamento adjuvante às cirurgias penetrantes e não-penetrantes para o glaucoma.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Angiogenesis Inhibitors/pharmacology , Bevacizumab/pharmacology , Glaucoma, Open-Angle/surgery , Methylcellulose/pharmacology , Angiogenesis Inhibitors/therapeutic use , Blister , Bevacizumab/therapeutic use , Chemotherapy, Adjuvant/methods , Drug Combinations , Drug Liberation , Feasibility Studies , Follow-Up Studies , Glaucoma, Open-Angle/drug therapy , Intraocular Pressure , Methylcellulose/therapeutic use , Pilot Projects , Prospective Studies , Slit Lamp , Wound Healing/drug effects
2.
Indian J Ophthalmol ; 2012 Mar; 60(2): 144-147
Article in English | IMSEAR | ID: sea-138812

ABSTRACT

Context: Pediatric cataract surgery is traditionally done with the aid of high-molecular-weight viscoelastics which are expensive. It needs to be determined if low-cost substitutes are just as successful. Aims: The study aims to determine the success rates for anterior and posterior capsulorrhexis and intraocular lens (IOL) implantation in the bag for pediatric cataract surgery performed with the aid of a low-molecular-weight viscoelastic. Settings and Design: Nonrandomized observational study. Materials and Methods: Children less than 6 years of age who underwent cataract surgery with IOL implantation in the period May 2008–May 2009 were included. The surgeries were done by pediatric ophthalmology fellows. A standard procedure of anterior capsulorrhexis, lens aspiration with primary posterior capsulorrhexis, anterior vitrectomy, and IOL implantation was followed. Three parameters were studied: successful completion of anterior and posterior capsulorrhexis and IOL implantation in the bag. Results: 33 eyes of 28 children were studied. The success rate for completion was 66.7% and 88.2 % for anterior and posterior capsulorrhexis, respectively. IOL implantation in the bag was successful in 87.9%. Conclusions: 2% hydroxypropylmethylcellulose is a viable low-cost alternative to more expensive options similar to high-molecular-weight viscoelastics. This is of great relevance to hospitals in developing countries.


Subject(s)
Capsulorhexis/economics , Capsulorhexis/instrumentation , Capsulorhexis/methods , Cataract , Child , Child, Preschool , Cost Savings , Fellowships and Scholarships/statistics & numerical data , Humans , Infant , Lens Implantation, Intraocular , Methylcellulose/analogs & derivatives , Methylcellulose/economics , Methylcellulose/therapeutic use , Ophthalmology/education , Ophthalmology/statistics & numerical data , Viscoelastic Substances/economics , Viscoelastic Substances/therapeutic use
3.
Article in English | IMSEAR | ID: sea-51803

ABSTRACT

Chewable tablets containing low dosage fluoride content were prepared using two varieties of celluloses and their in vitro parameters were evaluated. An eighteen month clinical trial revealed that both these formulations were effective in controlling the caries. However, ethyl cellulose is proved to be superior to methylcellulose as a controlled release matrix material in controlling caries. Thus this study recommends ethylcellulose matrix tablets containing low fluoride content is an efficacious and cost effective drug device in controlling dental caries.


Subject(s)
Administration, Oral , Cellulose/analogs & derivatives , Child , DMF Index , Delayed-Action Preparations , Dental Caries/drug therapy , Female , Fluorides, Topical/administration & dosage , Humans , Male , Methylcellulose/therapeutic use , Pharmaceutic Aids/therapeutic use , Sodium Fluoride/administration & dosage , Tablets
4.
Rev. argent. radiol ; 54(2): 107-13, abr.-jun. 1990. ilus
Article in Spanish | LILACS | ID: lil-122943

ABSTRACT

Se presenta la experiencia con 72 pacientes con diferentes patologías, en quienes se realizó tratamiento endovascular con embolización selectiva. Se discuten la técnica, diferentes materiales utilizados, resultados y complicaciones. Se concluye que la EE constituye una excelente alternativa terapéutica pre-quirúrgica, paliativa o definitiva, de fácil realización en centros especialmente entrenados


Subject(s)
Humans , Male , Female , Embolization, Therapeutic/methods , Aneurysm/therapy , Angiography , Contrast Media , Embolization, Therapeutic/adverse effects , Embolization, Therapeutic/instrumentation , Epistaxis/therapy , Gelatin Sponge, Absorbable/therapeutic use , Hematuria/therapy , Hemoptysis/therapy , Iodates , Kidney Neoplasms/therapy , Methylcellulose/therapeutic use , Palliative Care , Varicocele/therapy
6.
Rev. bras. oftalmol ; 47(6): 341-3, dez. 1988. ilus
Article in Portuguese | LILACS | ID: lil-73176

ABSTRACT

Apresentamos os resultados do uso de metilose 6% na capsulotomia anterior para cirurgia extracapsular da catarata


Subject(s)
Humans , Cataract Extraction , Methylcellulose/therapeutic use , Lenses, Intraocular
7.
Arq. bras. oftalmol ; 50(3): 120-3, 1987.
Article in Portuguese | LILACS | ID: lil-41424

ABSTRACT

Comparam-se os resultados de 100 facectomias extracapsulares com implante de LIO, utilizando metilcelulose a 2% somente sobre a incisäo (extra ocular), com os de outras técnicas já descritas. Observam que seus resultados também foram muito bons. Descrevem-se a técnica, que tem como principais vantagens a näo colocaçäo da metilcelulose dentro do olho e o impedimento à saída brusca da bolha de ar da câmara anterior


Subject(s)
Adult , Middle Aged , Humans , Lenses, Intraocular , Methylcellulose/therapeutic use
10.
Indian J Ophthalmol ; 1981 Jan; 28(4): 183-7
Article in English | IMSEAR | ID: sea-71877
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