Relevant bibliographies by topics / Sterilizing agent

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Sterilizing agent'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Sterilizing agent"

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Amantayev, Nurbolat Gabdullaevich, Marina Mikhailovna Silantyeva, and Vadim Tagirovich Khassanov. "Selecting sterilization conditions for the explants of different potato varieties to be in vitro introduced into the culture." Bulletin of the Karaganda University. “Biology, medicine, geography Series” 111, no. 3 (2023): 16–24. http://dx.doi.org/10.31489/2023bmg3/16-24.

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An explant is a fragment of plant tissue or organ that is incubated on its own or used to produce a primary callus. The introduction of any plant’s tissues into the culture in vitro begins with the selection of an uninfected viable explant. The authors presented the results of the effect of various sterilizing agents as well as the treatment timing on the viability of plant explants during microclonal propagation of potatoes of the following varieties: Aladin, Gala, Nevsky, Udacha and Kostanay Novosti. The meristem sprouts from potato tubers were used as parent material. The following commerci
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Hashim, Saiyidah Nafisah, Siti Zulaiha Ghazali, Norrizah Jaafar Sidik, Tay Chia-Chay, and Azani Saleh. "Surface sterilization method for reducing contamination of Clinacanthus nutans nodal explants intended for in-vitro culture." E3S Web of Conferences 306 (2021): 01004. http://dx.doi.org/10.1051/e3sconf/202130601004.

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Surface sterilization is a vital step in preparation of healthy and viable explants in tissue culture. Most surface contaminants can be eliminated by surface sterilization with a suitable sterilizing agent. The study aimed to present an effective disinfection method for Clinacanthus nutans shoot regeneration using nodal segments. A total of four different sterilization approaches were conducted by treating nodal explants with various concentrations of sterilizing agent. Sterilizing agents used were Rhizophora apiculata Pyroligneous acid (PA), sodium hypochlorite (Clorox) thiophanate-methyl (fu
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Belete, Yonas Zeslase, and Hagos Kalu. "Protocol Optimization for Surface Sterilization of Sugarcane Variety (B-52/298)." International Letters of Chemistry, Physics and Astronomy 48 (March 2015): 50–60. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.48.50.

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The aim of this study was to optimize conditions for surface sterilization of ex-plants of B-52/298 sugarcane cultivar variety. Experiment was carried out to determine the optimum concentrations of surface sterilizing agents and at what time they optimally sterilize. This experiment was conducted at MIT Plant Tissue Culture and Micro-propagation Laboratory Center, situated in Mekelle City. Three chemisterilants (Sodium Hypochlorite, Mercuric Chloride and Ethanol) were taken for the investigation. Three of the sterilizing agents were used in different concentrations at various time intervals an
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Belete, Yonas Zeslase, and Hagos Kalu. "Protocol Optimization for Surface Sterilization of Sugarcane Variety (B-52/298)." International Letters of Chemistry, Physics and Astronomy 48 (March 25, 2015): 50–60. http://dx.doi.org/10.56431/p-ta6564.

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The aim of this study was to optimize conditions for surface sterilization of ex-plants of B-52/298 sugarcane cultivar variety. Experiment was carried out to determine the optimum concentrations of surface sterilizing agents and at what time they optimally sterilize. This experiment was conducted at MIT Plant Tissue Culture and Micro-propagation Laboratory Center, situated in Mekelle City. Three chemisterilants (Sodium Hypochlorite, Mercuric Chloride and Ethanol) were taken for the investigation. Three of the sterilizing agents were used in different concentrations at various time intervals an
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Rakovsky, Slavcho, and Gennady Zaikov. "Application of Ozone in Medicine." Chemistry & Chemical Technology 3, no. 3 (2009): 237–48. http://dx.doi.org/10.23939/chcht03.03.237.

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This review deals with the application of ozone in medicine, its effects on the human organism and its use as a therapeutic approach and sterilizing agent. A particular attention is paid to the therapeutic properties, therapeutic dosage and scope of application. Some mechanisms of the ozone effect at exposure on different organs and systems in human body are also considered. Ozone toxicity is reviewed. The ozone use as a sterilizing agent in the pharmaceutical industry and cosmetics, as well as in the food processing industry is discussed.
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Neshumaeva, N. A., and M. A. Timina. "Selection of methods for sterilization of C. purpurea sclerotia for isolation of rye biosecurity agents." IOP Conference Series: Earth and Environmental Science 839, no. 4 (2021): 042010. http://dx.doi.org/10.1088/1755-1315/839/4/042010.

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Abstract Winter rye is a traditionally cultivated grain crop that is susceptible to ergot, a serious disease of the Poaceae family, caused by C. purpurea. Along with agrotechnical, organizational, and economic methods, biological control of ergot in grain crops is one of the ways to combat this disease. To isolate C. purpurea hyperparasites in a pure culture, the optimal sterilization options were selected, which were to exclude the infection of ergot sclerotia with saprophytic microflora. Before sterilization, C. purpurea were additionally washed in the running water with the addition of SAS
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B.M., Bhyravi, Athani S.I., D. P. Prakasha, et al. "Effect of sterilizing agent and seed treatment method on In vitro seed germination of guava cv. Arka Kiran." Ecology, Environment and Conservation 30, no. 02 (2024): 588–91. http://dx.doi.org/10.53550/eec.2024.v30i02.028.

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The in vitro germination of seeds of guava cv. Arka Kiran was mainly affected by contamination and seed coat dormancy. For successful in vitro germination of guava seeds, contamination control and breaking of seed dormancy are the two main steps one should fallow. An experiment on “Effect of sterilizing agent and seed treatment method on in vitro seed germination of guava cv. Arka Kiran” was carried out at College of Horticulture, Sirsi, Uttar Kannada, Karnataka during 2021-2023. The study revealed significant influence of different sterilizing agents and seed treatment method on contamination
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Markova, Marina, and Elena Somova. "Regeneration capacity of Cerasus fruticosa and Prunus domestica into the in vitro culture." Agrarian Bulletin of the 209, no. 06 (2021): 43–52. http://dx.doi.org/10.32417/1997-4868-2021-209-06-43-52.

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Abstract. The aim of these studies was to introduce into the in vitro culture the steppe cherry (Cerasus fruticosa) variety Shchedraya and the domestic plum (Prunus domestica) variety Sineokaya for subsequent micropropagation. Methods. Optimal conditions for obtaining viable explants, such as sterilizing agent and initiation time, have been investigated. The suitability of various nutrient media for in vitro cultivation of these cultures has also been tested. As a result of the experiments, it was revealed that the most effective sterilizing agents were 38 % perhydrol (control) and 6% chlorhex
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NAGASUPRIYA, T. VEERA, K. VENKATA LAXMI, P. SAIDAIAH, VEENA JOSHI, and M. GOPALA KRISHNA. "EFFECT OF DIFFERENT SURFACE STERILIZATION METHODS AND DIFFERENT PLANT GROWTH REGULATORS ON CULTURE ESTABLISHMENT FROM POMEGRANATE NODAL EXPLANTS OF cv. BHAGWA." Asian Journal of Microbiology, Biotechnology & Environmental Sciences 26, no. 04 (2024): 486–91. https://doi.org/10.53550/ajmbes.2024.v26i04.007.

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The present investigation was conducted to know the effect of different surface sterilization methods and different plant growth regulators on culture establishment from Pomegranate nodal explants of cv. Bhagwa with two factors: Sterilizing agents(S): 0.1% Mercuric chloride (HgCl2) and 1% Sodium hypochlorite (NaOCl) each at two different timing intervals i.e., 5 min and 10 min and growth regulators(G) G1: BAP 2 mg L-1, G2: Kinetin 2 mg L-1, G3: 2-ip 2 mg L-1, G4: zeatin 2 mg L-1). The results revealed that highest percentage of uncontamination was recorded in S2: 0.1% HgCl2 for 10min (93.33%)
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MARKOVA, M. G., and E. N. SOMOVA. "INITIATION OF HORTICULTURAL CROP EXPLANTS IN VITRO." Izvestiâ Timirâzevskoj selʹskohozâjstvennoj akademii, no. 4 (2022): 71–81. http://dx.doi.org/10.26897/0021-342x-2022-4-71-81.

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The stage of introduction into sterile culture plays an important role in clonal micropropagation. The purpose of these studies was to find the optimal sterilizing agent at the stage of introducing blue honeysuckle, red raspberry, garden strawberry, steppe cherry, house plum into in vitro culture, as well as the optimal nutrient medium at this stage for blue honeysuckle and red raspberry. As sterilizing agents with optimal exposure, the following were used: 48% ethyl alcohol (control) 8–10 min., 33% perhydrol 6–8 min., 6% chlorhexidine 8–10 min., 0.1% sublimate 1–2 min., 10.0% Domestos 6–7 min
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Dissertations / Theses on the topic "Sterilizing agent"

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Trahan, William R. "Peracetic Acid: A Practical Agent for Sterilizing Heat-Labile Polymeric Tissue-engineering Scaffolds." VCU Scholars Compass, 2015. http://scholarscompass.vcu.edu/etd/3728.

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Advanced biomaterials and sophisticated processing technologies aim to fabricate tissue-engineering scaffolds that can predictably interact within a biological environment at a cellular level. Sterilization of such scaffolds is at the core of patient safety and is an important regulatory issue that needs to be addressed prior to clinical translation. In addition, it is crucial that meticulously engineered micro- and nano- structures are preserved after sterilization. Conventional sterilization methods involving heat, steam and radiation are not compatible with engineered polymeric systems beca
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Books on the topic "Sterilizing agent"

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ANSI/AAMI/ISO 14937:2009/(R)2013; Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices. AAMI, 2009. http://dx.doi.org/10.2345/9781570203695.

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ANSI/AAMI/ISO 14160:2011/(R)2016; Sterilization of health care products — Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives — Requirements for characterization, development, validation and routine control of a sterilization process for medical devices. AAMI, 2011. http://dx.doi.org/10.2345/9781570204333.

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Book chapters on the topic "Sterilizing agent"

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Nelis, M., and J. Oleffe. "Occupational Contact Dermatitis from Glutaraldehyde Used as a Cold Sterilizing Agent." In Current Topics in Contact Dermatitis. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74299-6_17.

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Raman, Uma, and Vidyaa Iyer. "Chemicals, Disinfectants and Sterilizing Agents." In Going Green: A Manual of Waste Management for the Dental Practitioner. Jaypee Brothers Medical Publishers (P) Ltd., 2007. http://dx.doi.org/10.5005/jp/books/11034_13.

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Mascart, Françoise, Violette Dirix, and Camille Locht. "The human immune responses to pertussis and pertussis vaccines." In Pertussis. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198811879.003.0007.

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Two types of pertussis vaccines are currently available: the first-generation, whole-cell (wP) and more recent, acellular (aP) vaccines. The aP vaccine has replaced the wP vaccine in most industrialized countries, based on an improved safety profile and comparable efficacy of the former compared to the latter. As both vaccines, as well as prior infection, protect well against whooping cough disease, albeit by different mechanisms, the human immune responses to natural infection and vaccination have been extensively studied over the last decades. Shortly after the discovery of the causative age
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"Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices." In ANSI/AAMI/ISO 14937:2009/(R)2013; Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices. AAMI, 2009. http://dx.doi.org/10.2345/9781570203695.ch1.

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Mavhunga, Clapperton Chakanetsa. "How to Trap a Fly." In The Mobile Workshop. The MIT Press, 2018. http://dx.doi.org/10.7551/mitpress/9780262535021.003.0005.

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This chapter considers one of the stratagems developing out of an intelligence system of mhesvi, trapping systems. This approach was based on the underlying principle that the chipukanana had very small reproductive potential, that a slight reduction in the chipukanana's reproductive rate or increase in its mortality rate was enough to control its entire population. To do so, mhesvi had to be attracted to artificial baits laced with killing or sterilizing agents. These “attractant studies” targeted mhesvi's mobilities, sensory system, and feeding behavior; once attracted, the next step was to
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"Sterilization of health care products — Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives — Requirements for characterization, development, validation and routine control of a sterilization process for medical devices." In ANSI/AAMI/ISO 14160:2011/(R)2016; Sterilization of health care products — Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives — Requirements for characterization, development, validation and routine control of a sterilization process for medical devices. AAMI, 2011. http://dx.doi.org/10.2345/9781570204333.ch1.

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Conference papers on the topic "Sterilizing agent"

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Tanji, Y., S. Takano, K. Miyanaga, K. Hori, and H. Unno. "Antibacterial Activity of a Biocide (5-Chloro-2-Methyl-4-Isothiazolin-3-One; CMI) in Biofilm." In CORROSION 2004. NACE International, 2004. https://doi.org/10.5006/c2004-04577.

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Abstract Since 5-chloro-2-methyl-4-isothiazolin-3-one (CMI) has a relatively wide antibacterial spectrum, and low toxicity to humans, it is widely used as a bactericide and fungicide, or a slime control agent for a cooling tower. The minimum inhibitory concentration of CMI for E. coli K-12 was 1.6 mg/l. Short-time (~45 min) exposure of E. coli K-12 to 20 mg/l CMI prolonged the lag phase of cell growth. On the other hand, a normal logarithmic growth phase was observed after the lag phase. When E. coli K-12 was exposed to 1.0 mg/1 CMI for 25 h, the sterilization fraction reached 99%. A CMI conce
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Kukushkina, K. V. "Optimal sterilization conditions for obtaining viable explants." In III All-Russian (national) scientific conference with international participation “Russian science, innovation, education”. Krasoyarsk Science & Technology City Hall, 2024. http://dx.doi.org/10.47813/rosnio-iii.2024.1004.

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The conditions of sterilization of fragments of leaf plates of soft spring wheat for obtaining viable explants were evaluated. It was found that when using a sterilizing agent of different concentrations and exposure time, the proportion of samples that retained a green color is 0.38. The proportion of contamination of samples using a fifty percent solution of the commercial drug Bielizna (Sayanskkhimplast JSC, Russia) is 0.06. A statically significant dependence (p<0.0220) of the yellowing of the leaf plate on the concentration of the sterilizing agent was revealed when using a twenty-five
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Zhdanov, Aleksei E., Ilya M. Pahomov, and Alexey I. Ulybin. "Low-Temperature Plasma Sterilization: Using a Sterilizing Agent Based on Organic Acids (SterAcidAgent®)." In 2019 E-Health and Bioengineering Conference (EHB). IEEE, 2019. http://dx.doi.org/10.1109/ehb47216.2019.8970055.

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