Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas

<abstract language="eng">I) the A. presents a method developed for the preparation of thick blood films, specially old desiccated smears. The observations are based on the experience of more than 53000 blood samples collected in the laboratory of the “Serviço de Malaria do Nordeste”...

Full description

Bibliographic Details
Main Author: G. de Freitas
Format: Article
Language:English
Published: Instituto Oswaldo Cruz, Ministério da Saúde 1942-01-01
Series:Memórias do Instituto Oswaldo Cruz.
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761942000200004
id doaj-900d29dc2fff4a48889a87ab5ea6fbe2
record_format Article
spelling doaj-900d29dc2fff4a48889a87ab5ea6fbe22020-11-24T22:04:09ZengInstituto Oswaldo Cruz, Ministério da SaúdeMemórias do Instituto Oswaldo Cruz.0074-02761678-80601942-01-0137221922410.1590/S0074-02761942000200004Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecasG. de Freitas<abstract language="eng">I) the A. presents a method developed for the preparation of thick blood films, specially old desiccated smears. The observations are based on the experience of more than 53000 blood samples collected in the laboratory of the “Serviço de Malaria do Nordeste” as well as in the research department of the “Serviço de Malaria da Baixada Fluminenese”. II) As in introductory matter, he emphasizes the value of the obstacles presented by overdrying of the thick blood films occurring systematically in great malaria control organizations in which the laboratory receives materials from more or less remote localities, particularly in the Brazilian northeast, in regions invaded by Anopheles gambiae. III) An analysis of the causes of failure of the methods of Chorine and Knowles recorded in the literature for such purposes is given, as well as its adaptability for the simultaneous preparation of large numbers of samples. IV) The method is based the protective action of a previous fixation by a dilute solution of formalin, which, without preventing further dehemoglobinization, prevents morphological alterations in the parasites by the action of Knowles solution which is retained in this metod without modification. V) For washing out the acids of the dehemoglobinizating solution as well as for diluting the Giemsa stain, the A. proposes a very simple technique, extremely convenient for such purpose, which consists in adding acetic acid to the distilled water in the proportion of 1 drop for each 10cc of water, and then increasing the hydrogeni-on concentration to pH 7.2 with a 2% sol. of sodium carbonate. As indicator a 0.02% solution purple-bromcresol prepared in accordante to Medalia, is used. In this reaction there is the formation of the acetic acid &#8596; sodium acetate, buffer system very suitable for giving a convenient pH and for preventing the precipitation of the dye, which can be used for two or three batches of 700 or 800 slides each, without changing the staining solution. VI) – The method can be summarized as follow: For a small number of samples, Coplin’s or any other staining jar can be used. Large number of slides must be placed in groups of 10 or 15 units each, the slides being separated by a piece of cardboard, according to Barber & Komp. A) Fix in dilute formalin (2%), during 5 minutes. b) Without washing, put in Knowles solution (see the formula in the text), no more than 20 minutes. c)Two successive washings in distilled water, buffered as explained above (which can be used several times). d) Dry and stain with Giemsa solution, prepared by using 1 drop of the stain for each c. c. of buffered distilled water. Time: 1 hour. E) Was in distilled water and dry.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761942000200004
collection DOAJ
language English
format Article
sources DOAJ
author G. de Freitas
spellingShingle G. de Freitas
Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
Memórias do Instituto Oswaldo Cruz.
author_facet G. de Freitas
author_sort G. de Freitas
title Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
title_short Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
title_full Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
title_fullStr Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
title_full_unstemmed Sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
title_sort sobre o preparo dos parasitas da malária em distensões espessas, especialmente em amostras supersecas
publisher Instituto Oswaldo Cruz, Ministério da Saúde
series Memórias do Instituto Oswaldo Cruz.
issn 0074-0276
1678-8060
publishDate 1942-01-01
description <abstract language="eng">I) the A. presents a method developed for the preparation of thick blood films, specially old desiccated smears. The observations are based on the experience of more than 53000 blood samples collected in the laboratory of the “Serviço de Malaria do Nordeste” as well as in the research department of the “Serviço de Malaria da Baixada Fluminenese”. II) As in introductory matter, he emphasizes the value of the obstacles presented by overdrying of the thick blood films occurring systematically in great malaria control organizations in which the laboratory receives materials from more or less remote localities, particularly in the Brazilian northeast, in regions invaded by Anopheles gambiae. III) An analysis of the causes of failure of the methods of Chorine and Knowles recorded in the literature for such purposes is given, as well as its adaptability for the simultaneous preparation of large numbers of samples. IV) The method is based the protective action of a previous fixation by a dilute solution of formalin, which, without preventing further dehemoglobinization, prevents morphological alterations in the parasites by the action of Knowles solution which is retained in this metod without modification. V) For washing out the acids of the dehemoglobinizating solution as well as for diluting the Giemsa stain, the A. proposes a very simple technique, extremely convenient for such purpose, which consists in adding acetic acid to the distilled water in the proportion of 1 drop for each 10cc of water, and then increasing the hydrogeni-on concentration to pH 7.2 with a 2% sol. of sodium carbonate. As indicator a 0.02% solution purple-bromcresol prepared in accordante to Medalia, is used. In this reaction there is the formation of the acetic acid &#8596; sodium acetate, buffer system very suitable for giving a convenient pH and for preventing the precipitation of the dye, which can be used for two or three batches of 700 or 800 slides each, without changing the staining solution. VI) – The method can be summarized as follow: For a small number of samples, Coplin’s or any other staining jar can be used. Large number of slides must be placed in groups of 10 or 15 units each, the slides being separated by a piece of cardboard, according to Barber & Komp. A) Fix in dilute formalin (2%), during 5 minutes. b) Without washing, put in Knowles solution (see the formula in the text), no more than 20 minutes. c)Two successive washings in distilled water, buffered as explained above (which can be used several times). d) Dry and stain with Giemsa solution, prepared by using 1 drop of the stain for each c. c. of buffered distilled water. Time: 1 hour. E) Was in distilled water and dry.
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761942000200004
work_keys_str_mv AT gdefreitas sobreopreparodosparasitasdamalariaemdistensoesespessasespecialmenteemamostrassupersecas
_version_ 1725830216207564800