{"id":{"repo_id":"greece","oai_identifier":"oai:10442/1358"},"canonical_url":"https://search.dev.ndltd.org/etd/greece/oai:10442/1358","repository":{"repo_id":"greece","name":"Greek National Archive of PhD Theses","base_url":"https://phdtheses.ekt.gr/eadd_oai/request"},"display":{"title":"ΜΙΚΡΟΒΙΟΛΟΓΙΚΟΣ ΕΛΕΓΧΟΣ ΑΝΤΙΜΙΚΡΟΒΙΑΚΩΝ ΠΑΡΑΓΟΝΤΩΝ","abstract":"THE PRESENT STUDY IS DIVIDED INTO THREE PARTS: THE FIRST PART (ANTIBIOTICS), WAS UNDERTAKEN IN ORDER TO EVALUATE THE ANTIBACTERIAL ACTIVITY OF 9 ANTIBIOTICS IN VITRO. THEY WERE TESTED AGAINST 150 STRAINS OF P. AERUGINOSA, WHICH HAD BEEN ISOLATED FROM VARIOUS HOSPITALS OF ATHENS AREA, AND VARIOUS CLINICAL MATERIALS.SUSCEPTIBILITY TESTS OF THESE STRAINS TO THE ANTIBIOTICS WERE PERFORMED INDIVIDUALLY BY THE DETERMINATION OF MINIMUM INHIBITORY CONCENTRATIONS (MIC), USING ACONVENTIONAL AGAR DILUTION TECHNIQUE EMPLOYING MUELLER-HINTON AGAR. THE SUSCEPTIBILITY PERCENTAGES OF THE 150 STRAINS TO THE 9 ANTIBIOTICS TESTED WERE AS FOLLOWS: CIPROFLOXACIN 100%, CEFTAZADIME 88%, THIENAMYCIN 82%, AZTREONAM 81%, NALIDIXIC ACID 51%, CEFOTAXIM 41%, CARBENICILLIN 36%, GENTAMICIN 23% AND CLOROMPHENICOL 0%. IN THE SECOND PART OF THIS STUDY (ANTISEPTICS), WE EVALUATED THE ANTIBACTERIAL ACTIVITY OF 12 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN - O- PHENYLPHENOL), SODIUM LAURYL SULFATE, SODIUM LAURYL ETHER SULFATE, CETRIMIDE, MIRANOL C2M, MIRANOL CM, MIRANOL C2MSF, MIRANOL H2M, MIRATAINE BB AND MIRATAINE CB, USING THE DILUTION- NEUTRALIZATION METHOD (NF T72-50). THE TESTEDMICROORGANISMS WERE: S. AUREUS, STR. FAECALIS, E. COLI AND P. AERUGINOSA. IN THE THIRD PART (ANTIFUNGAL AGENTS), WE STUDIED 5 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN, CETRIMIDE), MIRANOL CM AND MIRABOL A 15. THEIR ACTIVITY WAS DETERMINED BY THE DILUTION- NEUTRALIZATION METHOD NF T72-200. THE TESTED MICROORGANISMS WERE: CANDIDA ALBICANS, ASPERGILLUS VERSICOLOR, PENICILLIUMVERRUCOSUM AND CLADOSPORIUM CLADOSPORIOIDES.","abstract_html":"THE PRESENT STUDY IS DIVIDED INTO THREE PARTS: THE FIRST PART (ANTIBIOTICS), WAS UNDERTAKEN IN ORDER TO EVALUATE THE ANTIBACTERIAL ACTIVITY OF 9 ANTIBIOTICS IN VITRO. THEY WERE TESTED AGAINST 150 STRAINS OF P. AERUGINOSA, WHICH HAD BEEN ISOLATED FROM VARIOUS HOSPITALS OF ATHENS AREA, AND VARIOUS CLINICAL MATERIALS.SUSCEPTIBILITY TESTS OF THESE STRAINS TO THE ANTIBIOTICS WERE PERFORMED INDIVIDUALLY BY THE DETERMINATION OF MINIMUM INHIBITORY CONCENTRATIONS (MIC), USING ACONVENTIONAL AGAR DILUTION TECHNIQUE EMPLOYING MUELLER-HINTON AGAR. THE SUSCEPTIBILITY PERCENTAGES OF THE 150 STRAINS TO THE 9 ANTIBIOTICS TESTED WERE AS FOLLOWS: CIPROFLOXACIN 100%, CEFTAZADIME 88%, THIENAMYCIN 82%, AZTREONAM 81%, NALIDIXIC ACID 51%, CEFOTAXIM 41%, CARBENICILLIN 36%, GENTAMICIN 23% AND CLOROMPHENICOL 0%. IN THE SECOND PART OF THIS STUDY (ANTISEPTICS), WE EVALUATED THE ANTIBACTERIAL ACTIVITY OF 12 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN - O- PHENYLPHENOL), SODIUM LAURYL SULFATE, SODIUM LAURYL ETHER SULFATE, CETRIMIDE, MIRANOL C2M, MIRANOL CM, MIRANOL C2MSF, MIRANOL H2M, MIRATAINE BB AND MIRATAINE CB, USING THE DILUTION- NEUTRALIZATION METHOD (NF T72-50). THE TESTEDMICROORGANISMS WERE: S. AUREUS, STR. FAECALIS, E. COLI AND P. AERUGINOSA. IN THE THIRD PART (ANTIFUNGAL AGENTS), WE STUDIED 5 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN, CETRIMIDE), MIRANOL CM AND MIRABOL A 15. THEIR ACTIVITY WAS DETERMINED BY THE DILUTION- NEUTRALIZATION METHOD NF T72-200. THE TESTED MICROORGANISMS WERE: CANDIDA ALBICANS, ASPERGILLUS VERSICOLOR, PENICILLIUMVERRUCOSUM AND CLADOSPORIUM CLADOSPORIOIDES.","abstract_has_math":false,"creators":["Tumah, Haitham","Τουμά, Χαϊθάμ"],"institution":"National and Kapodistrian University of Athens","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1988,"date_issued":"1988","date_published":"1988","updated_at":"2026-07-24T02:24:52Z","subjects":["Αντιβιοτικά","Αντιμυκητιακά","Αντισηπτικά","Απολυμαντικά","Antibiotics","ANTIFUNGI","ANTISEPTICS","Disinfectants","Ιατρική και Επιστήμες Υγείας","Βασική Ιατρική","Medical and Health Sciences","Basic Medicine"],"languages":["gre"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["10.12681/eadd/1358"],"render_values":[{"text":"10.12681/eadd/1358","href":"https://doi.org/10.12681/eadd/1358","code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/10442/hedi/1358","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Tumah, Haitham","Τουμά, Χαϊθάμ"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["1988"]},{"key":"dc:publisher","label":"Institution","values":["National and Kapodistrian University of Athens","Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)"]},{"key":"dc:type","label":"Dc Type","values":["PhD Thesis"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Αντιβιοτικά","Αντιμυκητιακά","Αντισηπτικά","Απολυμαντικά","Antibiotics","ANTIFUNGI","ANTISEPTICS","Disinfectants","Ιατρική και Επιστήμες Υγείας","Βασική Ιατρική","Medical and Health Sciences","Basic Medicine"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["gre"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["10.12681/eadd/1358","http://hdl.handle.net/10442/hedi/1358"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["THE PRESENT STUDY IS DIVIDED INTO THREE PARTS: THE FIRST PART (ANTIBIOTICS), WAS UNDERTAKEN IN ORDER TO EVALUATE THE ANTIBACTERIAL ACTIVITY OF 9 ANTIBIOTICS IN VITRO. THEY WERE TESTED AGAINST 150 STRAINS OF P. AERUGINOSA, WHICH HAD BEEN ISOLATED FROM VARIOUS HOSPITALS OF ATHENS AREA, AND VARIOUS CLINICAL MATERIALS.SUSCEPTIBILITY TESTS OF THESE STRAINS TO THE ANTIBIOTICS WERE PERFORMED INDIVIDUALLY BY THE DETERMINATION OF MINIMUM INHIBITORY CONCENTRATIONS (MIC), USING ACONVENTIONAL AGAR DILUTION TECHNIQUE EMPLOYING MUELLER-HINTON AGAR. THE SUSCEPTIBILITY PERCENTAGES OF THE 150 STRAINS TO THE 9 ANTIBIOTICS TESTED WERE AS FOLLOWS: CIPROFLOXACIN 100%, CEFTAZADIME 88%, THIENAMYCIN 82%, AZTREONAM 81%, NALIDIXIC ACID 51%, CEFOTAXIM 41%, CARBENICILLIN 36%, GENTAMICIN 23% AND CLOROMPHENICOL 0%. IN THE SECOND PART OF THIS STUDY (ANTISEPTICS), WE EVALUATED THE ANTIBACTERIAL ACTIVITY OF 12 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN - O- PHENYLPHENOL), SODIUM LAURYL SULFATE, SODIUM LAURYL ETHER SULFATE, CETRIMIDE, MIRANOL C2M, MIRANOL CM, MIRANOL C2MSF, MIRANOL H2M, MIRATAINE BB AND MIRATAINE CB, USING THE DILUTION- NEUTRALIZATION METHOD (NF T72-50). THE TESTEDMICROORGANISMS WERE: S. AUREUS, STR. FAECALIS, E. COLI AND P. AERUGINOSA. IN THE THIRD PART (ANTIFUNGAL AGENTS), WE STUDIED 5 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN, CETRIMIDE), MIRANOL CM AND MIRABOL A 15. THEIR ACTIVITY WAS DETERMINED BY THE DILUTION- NEUTRALIZATION METHOD NF T72-200. THE TESTED MICROORGANISMS WERE: CANDIDA ALBICANS, ASPERGILLUS VERSICOLOR, PENICILLIUMVERRUCOSUM AND CLADOSPORIUM CLADOSPORIOIDES.","Η ΜΕΛΕΤΗ ΑΥΤΗ ΔΙΑΙΡΕΙΤΑΙ ΣΕ ΤΡΙΑ ΜΕΡΗ: ΣΤΟ ΠΡΩΤΟ ΜΕΡΟΣ (ΑΝΤΙΒΙΟΤΙΚΑ), ΑΞΙΟΛΟΓΗΘΗΚΕ Η IN VITRO ΑΝΤΙΜΙΚΡΟΒΙΑΚΗ ΔΡΑΣΗ 9 ΑΝΤΙΒΙΟΤΙΚΩΝ ΚΑΤΑ 150 ΣΤΕΛΕΧΩΝ P. AERUGINOSA ΠΟΥ ΑΠΟΜΟΝΩΘΗΚΑΝ ΑΠΟ ΔΙΑΦΟΡΑ ΝΟΣΟΚΟΜΕΙΑ ΤΗΣ ΑΘΗΝΑΣ. Η ΕΛΑΧΙΣΤΗ ΑΝΑΣΤΑΛΤΙΚΗ ΠΥΚΝΟΤΗΤΑ (MIC) ΥΠΟΛΟΓΙΣΤΗΚΕ ΜΕ ΤΗ ΜΕΘΟΔΟ ΤΩΝ ΔΙΑΔΟΧΙΚΩΝ ΑΡΑΙΩΣΕΩΝ ΣΕ ΑΓΑΡ. ΠΡΟΕΚΥΨΕ ΟΤΙ Η ΕΠΙ ΤΟΙΣ ΕΚΑΤΟ ΕΥΑΙΣΘΗΣΙΑ ΤΩΝ ΣΤΕΛΕΧΩΝ ΑΥΤΩΝ ΣΤΑ ΕΞΕΤΑΣΤΕΑ ΑΝΤΙΒΙΟΤΙΚΑ ΗΤΑΝ Η ΕΞΗΣ: CIPROFLOXACIN 100%, CEFTAZADIME 88%, THIENAMYCIN 82%, AZTREONAM 81%, NALIDIXIC ACID 51%, CEFOTAXIME 41%, CARBENICILLIN 36%, GENTAMICIN 23% ΚΑΙ CHLORAMPHENICOL 0%. ΣΤΟ ΔΕΥΤΕΡΟ ΜΕΡΟΣ (ΑΝΤΙΣΗΠΤΙΚΑ), ΜΕΛΕΤΗΘΗΚΕ Η ΑΝΤΙΜΙΚΡΟΒΙΑΚΗ ΔΡΑΣΗ 12 ΧΗΜΙΚΩΝ ΕΝΩΣΕΩΝ (IRGASAN - O- PHENYLPHENOL), SODIUM LAURYL SULFATE, SODIUM LAURYL ETHER SULFATE, CETRIMIDE, MIRANOL C2M, MIRANOL CM, MIRANOL C2MSF, MIRANOL H2M, MIRATAINE BB ΚΑΙ MIRATAINE CB. Ο ΠΡΟΣΔΙΟΡΙΣΜΟΣ ΤΗΣ ΑΝΤΙΜΙΚΡΟΒΙΑΚΗΣ ΔΡΑΣΗΣ ΕΓΙΝΕ ΜΕ ΤΗ ΜΕΘΟΔΟ ΔΙΑΛΥΣΕΩΣ- ΕΞΟΥΔΕΤΕΡΩΣΕΩΣ NF T72-50. ΧΡΗΣΙΜΟΠΟΙΗΘΗΚΑΝ ΤΑ ΕΞΗΣ ΣΤΕΛΕΧΗ ΜΙΚΡΟΒΙΩΝ: S.AUREUS, STR. FAECALIS, E. COLI ΚΑΙ P. AERUGINOSA. ΣΤΟ ΤΡΙΤΟ ΜΕΡΟΣ (ΑΝΤΙΜΥΚΗΤΙΑΚΑ), ΕΛΕΓΧΘΗΚΕ Η ΑΝΤΙΜΙΚΡΟΒΙΑΚΗ ΔΡΑΣΗ 5 ΧΗΜΙΚΩΝ ΕΝΩΣΕΩΝ: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN - O- PHENYLPHENOL), MIRANOL CM ΚΑΙ MIRABOL A 15. Ο ΠΡΟΣΔΙΟΡΙΣΜΟΣ ΤΗΣ ΔΡΑΣΗΣ ΕΓΙΝΕ ΜΕ ΤΗ ΜΕΘΟΔΟ ΔΙΑΛΥΣΕΩΣ-ΕΞΟΥΔΕΤΕΡΩΣΕΩΣ NF T72-200. ΧΡΗΣΙΜΟΠΟΙΗΘΗΚΑΝ ΤΑ ΕΞΗΣ ΣΤΕΛΕΧΗ ΜΥΚΗΤΩΝ: CANDIDA ALBICANS, ASPERGILLUS VERSICOLOR, PENICILLIUM VERRUCOSUM ΚΑΙ CLADOSPORIUM CLADOSPORIOIDES."]},{"key":"dc:title","label":"Title","values":["ΜΙΚΡΟΒΙΟΛΟΓΙΚΟΣ ΕΛΕΓΧΟΣ ΑΝΤΙΜΙΚΡΟΒΙΑΚΩΝ ΠΑΡΑΓΟΝΤΩΝ","MICROBIOLOGICAL CONTROL OF ANTIBACTERIAL AGENTS"]}]}],"canonical_facts":{"dc:creator":["Tumah, Haitham","Τουμά, Χαϊθάμ"],"dc:date":["1988"],"dc:description":["THE PRESENT STUDY IS DIVIDED INTO THREE PARTS: THE FIRST PART (ANTIBIOTICS), WAS UNDERTAKEN IN ORDER TO EVALUATE THE ANTIBACTERIAL ACTIVITY OF 9 ANTIBIOTICS IN VITRO. THEY WERE TESTED AGAINST 150 STRAINS OF P. AERUGINOSA, WHICH HAD BEEN ISOLATED FROM VARIOUS HOSPITALS OF ATHENS AREA, AND VARIOUS CLINICAL MATERIALS.SUSCEPTIBILITY TESTS OF THESE STRAINS TO THE ANTIBIOTICS WERE PERFORMED INDIVIDUALLY BY THE DETERMINATION OF MINIMUM INHIBITORY CONCENTRATIONS (MIC), USING ACONVENTIONAL AGAR DILUTION TECHNIQUE EMPLOYING MUELLER-HINTON AGAR. THE SUSCEPTIBILITY PERCENTAGES OF THE 150 STRAINS TO THE 9 ANTIBIOTICS TESTED WERE AS FOLLOWS: CIPROFLOXACIN 100%, CEFTAZADIME 88%, THIENAMYCIN 82%, AZTREONAM 81%, NALIDIXIC ACID 51%, CEFOTAXIM 41%, CARBENICILLIN 36%, GENTAMICIN 23% AND CLOROMPHENICOL 0%. IN THE SECOND PART OF THIS STUDY (ANTISEPTICS), WE EVALUATED THE ANTIBACTERIAL ACTIVITY OF 12 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN - O- PHENYLPHENOL), SODIUM LAURYL SULFATE, SODIUM LAURYL ETHER SULFATE, CETRIMIDE, MIRANOL C2M, MIRANOL CM, MIRANOL C2MSF, MIRANOL H2M, MIRATAINE BB AND MIRATAINE CB, USING THE DILUTION- NEUTRALIZATION METHOD (NF T72-50). THE TESTEDMICROORGANISMS WERE: S. AUREUS, STR. FAECALIS, E. COLI AND P. AERUGINOSA. IN THE THIRD PART (ANTIFUNGAL AGENTS), WE STUDIED 5 CHEMICAL COMPOUNDS: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN, CETRIMIDE), MIRANOL CM AND MIRABOL A 15. THEIR ACTIVITY WAS DETERMINED BY THE DILUTION- NEUTRALIZATION METHOD NF T72-200. THE TESTED MICROORGANISMS WERE: CANDIDA ALBICANS, ASPERGILLUS VERSICOLOR, PENICILLIUMVERRUCOSUM AND CLADOSPORIUM CLADOSPORIOIDES.","Η ΜΕΛΕΤΗ ΑΥΤΗ ΔΙΑΙΡΕΙΤΑΙ ΣΕ ΤΡΙΑ ΜΕΡΗ: ΣΤΟ ΠΡΩΤΟ ΜΕΡΟΣ (ΑΝΤΙΒΙΟΤΙΚΑ), ΑΞΙΟΛΟΓΗΘΗΚΕ Η IN VITRO ΑΝΤΙΜΙΚΡΟΒΙΑΚΗ ΔΡΑΣΗ 9 ΑΝΤΙΒΙΟΤΙΚΩΝ ΚΑΤΑ 150 ΣΤΕΛΕΧΩΝ P. AERUGINOSA ΠΟΥ ΑΠΟΜΟΝΩΘΗΚΑΝ ΑΠΟ ΔΙΑΦΟΡΑ ΝΟΣΟΚΟΜΕΙΑ ΤΗΣ ΑΘΗΝΑΣ. Η ΕΛΑΧΙΣΤΗ ΑΝΑΣΤΑΛΤΙΚΗ ΠΥΚΝΟΤΗΤΑ (MIC) ΥΠΟΛΟΓΙΣΤΗΚΕ ΜΕ ΤΗ ΜΕΘΟΔΟ ΤΩΝ ΔΙΑΔΟΧΙΚΩΝ ΑΡΑΙΩΣΕΩΝ ΣΕ ΑΓΑΡ. ΠΡΟΕΚΥΨΕ ΟΤΙ Η ΕΠΙ ΤΟΙΣ ΕΚΑΤΟ ΕΥΑΙΣΘΗΣΙΑ ΤΩΝ ΣΤΕΛΕΧΩΝ ΑΥΤΩΝ ΣΤΑ ΕΞΕΤΑΣΤΕΑ ΑΝΤΙΒΙΟΤΙΚΑ ΗΤΑΝ Η ΕΞΗΣ: CIPROFLOXACIN 100%, CEFTAZADIME 88%, THIENAMYCIN 82%, AZTREONAM 81%, NALIDIXIC ACID 51%, CEFOTAXIME 41%, CARBENICILLIN 36%, GENTAMICIN 23% ΚΑΙ CHLORAMPHENICOL 0%. ΣΤΟ ΔΕΥΤΕΡΟ ΜΕΡΟΣ (ΑΝΤΙΣΗΠΤΙΚΑ), ΜΕΛΕΤΗΘΗΚΕ Η ΑΝΤΙΜΙΚΡΟΒΙΑΚΗ ΔΡΑΣΗ 12 ΧΗΜΙΚΩΝ ΕΝΩΣΕΩΝ (IRGASAN - O- PHENYLPHENOL), SODIUM LAURYL SULFATE, SODIUM LAURYL ETHER SULFATE, CETRIMIDE, MIRANOL C2M, MIRANOL CM, MIRANOL C2MSF, MIRANOL H2M, MIRATAINE BB ΚΑΙ MIRATAINE CB. Ο ΠΡΟΣΔΙΟΡΙΣΜΟΣ ΤΗΣ ΑΝΤΙΜΙΚΡΟΒΙΑΚΗΣ ΔΡΑΣΗΣ ΕΓΙΝΕ ΜΕ ΤΗ ΜΕΘΟΔΟ ΔΙΑΛΥΣΕΩΣ- ΕΞΟΥΔΕΤΕΡΩΣΕΩΣ NF T72-50. ΧΡΗΣΙΜΟΠΟΙΗΘΗΚΑΝ ΤΑ ΕΞΗΣ ΣΤΕΛΕΧΗ ΜΙΚΡΟΒΙΩΝ: S.AUREUS, STR. FAECALIS, E. COLI ΚΑΙ P. AERUGINOSA. ΣΤΟ ΤΡΙΤΟ ΜΕΡΟΣ (ΑΝΤΙΜΥΚΗΤΙΑΚΑ), ΕΛΕΓΧΘΗΚΕ Η ΑΝΤΙΜΙΚΡΟΒΙΑΚΗ ΔΡΑΣΗ 5 ΧΗΜΙΚΩΝ ΕΝΩΣΕΩΝ: IRGASAN DP300, O-PHENYLPHENOL, (IRGASAN - O- PHENYLPHENOL), MIRANOL CM ΚΑΙ MIRABOL A 15. Ο ΠΡΟΣΔΙΟΡΙΣΜΟΣ ΤΗΣ ΔΡΑΣΗΣ ΕΓΙΝΕ ΜΕ ΤΗ ΜΕΘΟΔΟ ΔΙΑΛΥΣΕΩΣ-ΕΞΟΥΔΕΤΕΡΩΣΕΩΣ NF T72-200. ΧΡΗΣΙΜΟΠΟΙΗΘΗΚΑΝ ΤΑ ΕΞΗΣ ΣΤΕΛΕΧΗ ΜΥΚΗΤΩΝ: CANDIDA ALBICANS, ASPERGILLUS VERSICOLOR, PENICILLIUM VERRUCOSUM ΚΑΙ CLADOSPORIUM CLADOSPORIOIDES."],"dc:identifier":["10.12681/eadd/1358","http://hdl.handle.net/10442/hedi/1358"],"dc:language":["gre"],"dc:publisher":["National and Kapodistrian University of Athens","Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)"],"dc:subject":["Αντιβιοτικά","Αντιμυκητιακά","Αντισηπτικά","Απολυμαντικά","Antibiotics","ANTIFUNGI","ANTISEPTICS","Disinfectants","Ιατρική και Επιστήμες Υγείας","Βασική Ιατρική","Medical and Health Sciences","Basic Medicine"],"dc:title":["ΜΙΚΡΟΒΙΟΛΟΓΙΚΟΣ ΕΛΕΓΧΟΣ ΑΝΤΙΜΙΚΡΟΒΙΑΚΩΝ ΠΑΡΑΓΟΝΤΩΝ","MICROBIOLOGICAL CONTROL OF ANTIBACTERIAL AGENTS"],"dc:type":["PhD Thesis"]},"updated_at":"2026-07-24T02:24:52Z"}