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This study explored the preservation effect of strigolactone analogs on Gastrodia elata tubers and screened out the suitable preservation measures of G. elata to provide a safer and more effective method for its storage and preservation. Fresh G. elata tubers were treated with 7FGR24, 2,4-D isooctyl ester, and maleic hydrazide, respectively. The growth of flower buds, the activities of CAT, and MDA, and the content of gastrodin and p-hydroxybenzyl alcohol were measured to compare the effects of different compounds on the storage and preservation of G. elata. The effects of different storage temperatures on the preservation of 7FGR24 were compared and analyzed. The gibberellin signal transduction receptor gene GeGID1 was cloned, and the effect of 7FGR24 on the expression level of GeGID1 was analyzed by quantitative polymerase chain reaction(qPCR). The toxicity of the G. elata preservative 7FGR24 was analyzed by intragastric administration in mice to evaluate its safety. The results showed that compared with 2,4-D isooctyl ester and maleic hydrazide, 7FGR24 treatment had a significant inhibitory effect on the growth of G. elata flower buds, and the CAT enzyme activity of G. elata was the highest, indicating that its preservation effect was stronger. Different storage temperatures had different effects on the preservation of G. elata, and the preservation effect was the strongest at 5 ℃. The open reading frame(ORF) of GeGID1 gene was 936 bp in length, and its expression level was significantly down-regulated after 7FGR24 treatment, indicating that 7FGR24 may inhibit the growth of flower buds by inhibiting the gibberellin signal of G. elata, thereby exerting a fresh-keeping effect. Feeding preservative 7FGR24 had no significant effect on the behavior and physiology of mice, indicating that it had no obvious toxicity. This study explored the application of the strigolactone analog 7FGR24 in the storage and preservation of G. elata and preliminarily established a method for the storage and preservation of G. elata, laying a foundation for the molecular mechanism of 7FGR24 in the storage and preservation of G. elata.
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Animals , Mice , Gastrodia , Gibberellins , Maleic Hydrazide , EstersABSTRACT
【Objective】 To study the effects of different storage temperature and different storage time on the activity of key growth factors in platelet-rich plasma(PRP), and to provide a theoretical basis for maximize the role of PRP in clinical treatment. 【Methods】 PRP was collected by blood cell isolation and apheresis, stored at 22℃ and -80℃, respectively. VEGF, TGF-β and PDGF were detected by ELISA. The content of growth factors in PRP was detected when stored at 22℃for 1, 3 and 5 days, and the growth factors content of PRP stored at 22℃ for 3 days was detected after thrombin activation for 0.5, 1 and 1.5 hours. The content of growth factor in frozen PRP (stored at -80℃ for 30 days after initial 3-days storage at 22℃ ) and fresh PRP (stored at 22℃ for 3 days) was compared. The growth factor content in PRP frozen at - 80℃ for 30, 60 and 180 days, and the growth factor content in PRP frozen at -80℃ for 180 days after repeated freeze-thaw for 1, 2, 3, 5 and 10 times were detected. 【Results】 The growth factor content of apheresis PRP was significantly higher than that of platelet-poor plasma. No statistical difference was noticed in VEGF, TGF-β and PDGF content in PRP at 1, 3 and 5 days stored at 22℃; no statistical difference was noticed in VEGF, TGF-β and PDGF content in PRP stored at 22℃ for 3 days after thrombin activation for 0.5, 1 and 1.5 hours. There was no statistically significant difference in growth factor content between PRP stored at 22℃ for 3 days versus frozen at -80℃ for 30 days after initial 3-days storage at 22℃. No statistical difference was found in VEGF, TGF-β and PDGF contents in frozen PRP repeatedly frozen and thawed for 1 to 10 times. 【Conclusion】 Apheresis PRP can release a large amount of growth factors after activation. Fresh PRP stored at 22℃ for 5 days or frozen at -80℃ for 180 days has no impact on the content of growth factors, and frozen PRP at -80℃ can achieve long-term, effective and safe preservation, which is conducive to multiple use of PRP in treatment.
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OBJECTIVES@#To investigate the effects of injury time, postmortem interval (PMI) and postmortem storage temperature on mRNA expression of glycoprotein non-metastatic melanoma protein B (Gpnmb), and to establish a linear regression model between Gpnmb mRNA expression and injury time, to provide aimed at providing potential indexes for injury time estimation.@*METHODS@#Test group SD rats were anesthetized and subjected to blunt contusion and randomly divided into 0 h, 4 h, 8 h, 12 h, 16 h, 20 h and 24 h groups after injury, with 18 rats in each group. After cervical dislocation, 6 rats in each group were collected and stored at 0 ℃, 16 ℃ and 26 ℃, respectively. The muscle tissue samples of quadriceps femoris injury were collected at 0 h, 12 h and 24 h postmortem at the same temperature. The grouping method and treatment method of the rats in the validation group were the same as above. The expression of Gpnmb mRNA in rat skeletal muscle was detected by RT-qPCR. The Pearson correlation coefficient was used to evaluate the correlation between Gpnmb mRNA expression and injury time, PMI, and postmortem storage temperature. SPSS 25.0 software was used to construct a linear regression model, and the validation group data was used for the back-substitution test.@*RESULTS@#The expression of Gpnmb mRNA continued to increase with the prolongation of injury time, and the expression level was highly correlated with injury time (P<0.05), but had little correlation with PMI and postmortem storage temperature (P>0.05). The linear regression equation between injury time (y) and Gpnmb mRNA relative expression (x) was y=0.611 x+4.489. The back-substitution test proved that the prediction of the model was accurate.@*CONCLUSIONS@#The expression of Gpnmb mRNA is almost not affected by the PMI and postmortem storage temperature, but is mainly related to the time of injury. Therefore, a linear regression model can be established to infer the time of injury.
Subject(s)
Animals , Rats , Glycoproteins , Linear Models , Melanoma , Membrane Glycoproteins/genetics , Postmortem Changes , Rats, Sprague-Dawley , RNA, Messenger/metabolism , Time FactorsABSTRACT
@#The properties of adhesives and light-cured resin composites are closely related to the repair of dental defects. Therefore, improving the properties of adhesives and resins composite to increase the success rate of filling has been the focus of research in the field of prosthodontics in recent years. Current studies have confirmed that temperature can change the properties of adhesives and light-cured resin composites, affecting their repair effect. A proper storage temperature ensures the good performance of materials: the self-etching adhesive system should be refrigerated, and the light-cured resin composite should be refrigerated or stored at room temperature according to its composition, proportion and other properties; however, the appropriate storage temperature for the etch-and-rinse adhesive system is not clear. The appropriate application temperature could improve the fluidity, monomer conversion, bonding strength, compressive strength and other properties of the materials to improve the quality of filling restoration. However, there is a wide variety of adhesives and resin composites, and the effect of temperature on each material is different. Thus, it is still necessary to explore the temperature range for material storage, precooling and preheating. Few studies have been performed in vivo, and the clinical restorative effects of adhesives and resin composites stored and used at different temperatures need to be further studied.
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【Objective】 To verify the results of HBV DNA and HCV RNA screening under different brands of vacuum collection tubes for blood samples, storage temperature and storage time. 【Methods】 Experiment 1 was conducted as follows: blood samples were collected simultaneously from 52 voluntary blood donors using two brands(divided into group A and group B) of vacuum collection tubes for blood samples. The plasma separation of group A and group B were compared, and the effects of storage time on the NAT yield of HBV DNA and HCV RNA were statistically analyzed. Experiment 2 was conducted as follows: the effects of different storage temperature, time and tubes on the NAT yield of HBV DNA and HCV RNA samples with low viral load in group A and B were verified and compared in the simulated phlebotomy condition. 【Results】 In Experiment 1: After centrifugation, blood plasma layer and cells layer were separated completely in group A(100%, 52/52), but one sample was not well separated in group B(1/52, 1.92%). After 4 to 10 h after collection, blood samples of two groups were centrifuged and screened for HBV DNA, HCV RNA within 24 h. No positive samples were yielded and the Ct values of internal control(IC-DNA and IC-RNA) were uniform. In Experiment 2: Whole blood samples, stored for either 4 h or 6~10 h at 4 ℃ or 25℃ before centrifugation, showed no difference on the NAT-yield of HBV DNA nor HCV RNA samples with low viral load(P>0.05). Ct values of HBV DNA and HCV RNA of group A was similar to those of group B as centrifuged samples were stored for 24 h or 72~104 h at 4℃(P>0.05), but all increased as the storage time prolonged. Ct values of HBV DNA in group A increased from 33.45±0.29(24 h) to 33.82±0.08(72~104 h) and HCV RNA from 35.21±0.20 to 36.12±0.43; HBV DNA from 33.46±0.25 to 34.30±0.60 and HCV RNA from 35.47±0.24 to 36.49±0.51 in group B. 【Conclusion】 Under certain laboratory condition, different storage time, storage temperature and tubes shed few effect on the NAT-yield of HBV DNA and HCV RNA samples with low virus loads. However, it is suggested that the blood sample be detected within 72 h after centrifugation at 4 ℃ storage.
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OBJECTIVE: To investigate the effect of temperature and time on the detection results of calcium and magnesium in urinary sample storage. METHODS: Urinary samples of 5 health volunteers were collected. The samples were stored in room temperature, 4 ℃ and-20 ℃ for different duration after sealed separately. A flame atomic absorption spectrometry was used to detect calcium and magnesium mass concentrations in the urinary samples. RESULTS: The variation rate of calcium and magnesium mass concentrations was <2.00% when urinary samples were stored at room temperature for 8 hours, the variation rate was <6.00% when samples were stored at 4 ℃ for 15 days, and it was <5.00% when samples were stored at-20 ℃ for 60 days. CONCLUSION: The temperature and time of urinary sample storage can affect the detection results of calcium and magnesium mass concentrations. Packing and storing samples at low temperature after collection as soon as possible is beneficial to ensure the accuracy of test results.
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Objective: To carry out effective management for the cold-chain temperature of in vitro diagnostic reagent so as to provide safe and credible inspection basis for clinical diagnosis and treatment. Methods: The remote control and alarm platform of cold storage and refrigerator were applied to achieve acceptance for temperature control of in vitro diagnostic reagent, and achieve acceptance for temperature and achieve differentiation management for unqualified product. These methods could ensure controllability of temperature for the reagent with requirements of cold-chain. Results: Through the management of cold-chain of in vitro diagnostic reagents, hospital has achieved effective supervising for them, and hospital has concrete record for these reagents in the entire medical process, and all of them were traceability. Therefore, it provide effective guarantee for clinical safety. Conclusion: The support of informatization technique and implementation of management system of hospital can ensure the cold-chain management of entire process is not out of control, and enhance the stability and accuracy of clinical test results and effective guarantee the safety of diagnosis and treatment for hospital.
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OBJECTIVE:To preliminarily study the stability of 3 pieces of Chinese medicinal formula(CMF)after decoction, and provide reference for guaranteeing storage quality of decocted liquid and improving safety of drug use. METHODS:3 represen-tative formulas of Gegen Huangqin Huanglian decoction(A formula),Wuling powder(B formula)and Didang decoction(C for-mula)from Shanghan Zabing Lun were selected,the decocted liquid were stored under ambient temperature(25 ℃)and refrigerat-ed temperature (4 ℃) after decocting by automatic boiling-machine and packing. The microorganism,precipitation,pH and con-tents of total flavonoids,alkaloid,polysaccharide,total protein after 1,7,14,21,28 d were detected. RESULTS:Compared with the first day,contents of total flavonoids,polysaccharide in formula A at ambient temperature group were significantly in-creased on the 28th(P<0.05),content of polysaccharide in refrigerated temperature group was significantly increased(P<0.05). Content of polysaccharide in formula B at ambient temperature group was significantly decreased(P<0.05). The pH and content of total flavonoids in formula C at ambient temperature group and refrigerated temperature group were significantly increased (P<0.05 or P<0.01). Other indexes showed no obvious changes during the trial period. CONCLUSIONS:Under ambient temperature and refrigerated temperature,liquid ingredients of above decocted CMF will change when storing for 4 weeks. It indicates that the storage time of decocted CMF should not be more than 3 weeks.
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Objective To study the effect of time and temperature on the count of peripheral blood cells in newborns.Methods The peripheral blood of 100 cases of newborns who were admitted in the First Affiliated Hospital of Hebei North University from January 2016 to June 2016 were collected,and measured with Sysmex XS-500i automatic blood cell analyzer immediately,then were split into two parts and stored at 4 ℃ and room temperature respectively.The measurement was repeated in 24 and 48 h,and the groups were compared on WBC,RBC,PLT,HGB,IG％ and IG#.Results There were statistically significant differences between the instantly measuring result and those in 24 and 48 h under room temperature (P＜0.05).In case of 4 ℃,the instantly measuring result had no obvious difference with that in 24 h (P＞0.05),while statistical difference with that in 48 h (P＜0.05).Conclusion Newborns' peripheral blood can be stored at 4 ℃C,and the counting results will not be affected for WBC,RBC,PLT,HGB,IG％ and IG# within 24 h.
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Objective To select the best storage temperature and accurate detection way of the blood alcohol content of drunk driving and provide technical support of judging objectively drunk driving behaviors for traffic management department. Methods This study selects EDTA-2 vacuum tubes, take human vein blood after drinking and respectively store at four temperature conditions -20℃、4℃~8 ℃、 25 ℃ normal temperature and high temperature of 35℃~42 ℃.GC method is used by testing 0,3d, 7d, 14d, 21d and 28d blood alcohol content, and the test result statistics and data are compared and analyzed. Results The blood alcohol contents within 0-3d stored at 35℃~42 ℃and 25 ℃temperature remain stable, decrease significantly after 3d (P<0.05); the blood alcohol contents stored at 4℃~8 ℃ temperature in 0~14d is basically stable and decrease significantly after 14d (P<0.05); at -20℃temperature there are no significant differences among the 28d testing results of blood alcohol contents. Conclusions It is suggested that the blood samples should be collected at low temperature and the best preservation temperature of blood samples is -20℃.
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Aims: Turkish white pickled cheese is the most consumed cheese type in Turkey and it is an important food to be evaluated in terms of food safety. In this study we investigated the behavior (survival and production of enterotoxin) of Staphylococcus aureus (S. aureus) NCTC 10654 in Turkish white pickled cheeses, which were ripened at 4 °C and 12 °C for 90 days. Methodology and results: Counting of microorganisms was carried out by conventional methods on appropriate media. Detection of enterotoxins was performed by double-sandwich ELISA technique and gene region responsible for enterotoxin production by reverse transcription-PCR (RT-PCR). The counts of S. aureus decreased (p 0.05). Staphylococcal enterotoxin could not be detected in the cheeses during ripening. Staphylococcal enterotoxin (SE) B mRNA was detected in cheese samples on days 1, 15, and 30 of ripening by RT-PCR. The SEB mRNA expression levels had differed according to the storage temperature. Conclusion, significance and impact of study: This study showed that enterotoxin B producing S. aureus decreased in Turkish white pickled cheese stored at different temperatures and it could not produce enterotoxins, possibly due to factors such as type and nature of the cheese, and the conditions of production and activity of the starter culture.
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[ ABSTRACT] AIM:To investigate the effect of storage temperature in renal biopsy tissue frozen section on immu-nofluorescence results.METHODS:One hundred renal biopsy samples of Zhejiang Province People’ s Hospital from Janu-ary to June, 2015 were enrolled.Two sets of cutting slices were stored in -70 ℃ low temperature refrigerator as experi-mental group and in -12 ℃ freezing cryostat as control group.The immunoglobulins ( IgG, IgA and IgM) and comple-ments (C3, C4 and C1q) as well as fibrinogen were detected with direct immunofluorescence in the next day.The typeⅣcollagen a3 and a5 chains were also detected by indirect immunofluorescence, and the qualitative and semi-quantitative re-sults were observed under the fluorescence microscope.RESULTS:There were 16 cases of 3+~4+IgG in the experi-mental group, while the corresponding IgG was all 1+~2+in control group, significantly weaker than that in experimen-tal group.There were 99 cases of 3+~4+a3 and 3+~4+a5 in experimental group, white there were 92 cases of 1+~2+a3/a5 and 8 cases negative in control group.The positive intensity was decreased in control group with statistical difference between the 2 groups ( P<0.05) .There were 15 cases of 4+IgA, 19 cases of 3+IgA, 15 cases of 3+IgM, 11 cases of 2+IgM, 13 cases of 4+C3, and 12 cases of 3+C3 in experimental group.The control group were similar to the results of experimental group, and no difference between the 2 groups was observed.CONCLUSION:The immunoflu-orescence results of renal biopsy frozen sections are highly affected by the section storage temperature, which has greater in-fluence on the immunofluorescence positive intensity of IgG and typeⅣcollagen.The renal biopsy frozen section should be stored in -70 ℃low temperature refrigerator.
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OBJECTIVE:To observe the effect of room temperature and low temperature storage on the chronergy of domes-tic cisatracurium. METHODS:90 patients undergoing elective surgery under general anesthesia were randomly divided into low tem-perature group,room temperature A group and room temperature B group,with 30 cases in each groups. Through single supramaxi-mal electrical stimulation of the adductor pollicis muscle,TOF-Watch SX muscle relaxation monitor was used to observe the degree of muscle relaxation. After induction of anesthesia and lost consciousness,the patients was given intravenous injection of cisatracu-rium 0.2 mg/kg;when muscle twitch decreased to the maximum inhibition degree,the patient received endotracheal intubation. The cisatracurium of low temperature group was stored in refrigerator at 2 to 5℃;that of room temperature A group and room tempera-ture B group was stored in incubator for 15 days or 30 days. The onset time,maximum inhibition degree of muscle twitch,clini-cal duration,recovery index and total chronergy were recorded in 3 groups. RESULTS:The maximal inhibition degree of muscle twitch reached 0 under the action of cisatracurium. There was no statistical significance in onset time and clinical duration between room temperature A group,room temperature B group and low temperature group(P>0.05);the recovery index and total chroner-gy of room temperature A group and room temperature B group were or longer than low temperature group,with statistical signifi-cance(P<0.05). CONCLUSIONS:Domestic cisatracurium stored at low temperature shows weaker effect on muscle relaxation.
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O leite de cabra é produzido em pequena escala, o que torna necessária sua estocagem, permitida pela legislação brasileira. O presente trabalho teve por objetivo avaliar a ação do resfriamento e congelamento sobre as características físico-químicas e microbiológicas do leite de cabra. Não foi observada variabilidade nos valores médios de acidez, estabilidade ao álcool, densidade, gordura, proteína, sólidos totais e lactose após armazenamento sob frio. Não foi observada instabilidade ao calor em nenhuma das amostras analisadas. Verificou-se tendência à diminuição na contagem de células somáticas (CSS) no leite congelado em relação ao fresco e ao refrigerado. A quantificação (NMP) de coliformes totais e termotolerantes variou de < 3 (ausência de crescimento) à > 1.100 UFC/mL, independentemente do armazenamento. Entretanto, determinou-se contagem de coliformes totais e termotolerantes significativamente maior (p < 0,0001) nas amostras mantidas sob refrigeração. Na prova de lactofermentação, observaram-se coágulos digeridos, floculosos e sulcados sem estabelecer correlação entre estes e a contagem bacteriana. A CCS e a contagem microbiana são critérios adotados no pagamento pela qualidade no leite caprino, e a temperatura de armazenamento pode influir sobre elas.(AU)
The small-scale goat milk production requires its storage, and such operation is allowed by Brazilian laws. This study aimed at evaluating the cooling and freezing effects on physical-chemical and microbiological characteristics of goat milk. However, no variability was verified in average acidity, alcohol stability, density, fat protein, total solids and lactose values after cold storage. Heat instability was not observed in any of the analyzed samples. There was a decreasing tendency in the somatic cell count (SCC) of frozen milk in comparison to fresh and refrigerated milk. The quantification (NMP) of total and thermo-tolerant coliforms varies from < 3 (no growth) to > 1,100 UFC/mL, regardless of the storage method. However, a slightly higher count (p < 0.0001) was observed for total and thermo-tolerant coliforms in the samples kept under refrigeration. In the lacto-fermentation test, digested, flocculated and grooved clots were observed without establishing a correlation between them and the bacterial count. SCC and microbial count are the criteria adopted when paying for the quality of goat milk, and the storage temperature may affect these criteria.(AU)
Subject(s)
Humans , Animals , Bacteria , Goats , Milk/microbiology , Cooled Foods , Food Storage , Pollution IndicatorsABSTRACT
Los componentes activos del polen a partir del cual se obtienen los extractos alergénicos pueden variar considerablemente deacuerdo al momento, el lugar dónde se recolecta y el períodocomprendido entre la recolección y su utilización.El presente trabajo pretende evaluar si la temperatura de conservacióndel grano de polen influye en la expresión de proteínasy en la antigenicidad de las mismas, al momento de prepararun extracto alergénico. La especie elegida para estudio fue Chenopodiumalbum L. ya que es de gran interés alergológico en laciudad de Bahía Blanca. Los granos de polen se conservaron a temperatura ambiente, 4 °Cy -18 °C por el término de dos meses. El contenido proteico de losextractos se determinó por el Método de Bradford. La expresiónproteica y la antigenicidad se estudiaron mediante electroforesisvertical Tricina-PAGE-SDS 12, 5 % e Inmunoblot respectivamente.Los resultados obtenidos demuestran que la concentración proteicatotal fue menor para los extractos obtenidos del polen conservadoa temperatura ambiente que para las otras dos condiciones.La expresión de proteínas varía cuantitativamente en todoslos extractos y si bien la expresión cualitativa prácticamente seconserva, aparece para el polen conservado a temperatura ambiente,una banda de PM menor a 12 kDa. Esta banda podríaser consecuencia de la degradación proteica que experimenta elpolen a esa temperatura de almacenamiento. En cuanto a la antigenicidadde los extractos no hay diferencias cualitativas aunquepueden apreciarse diferencias cuantitativas significativas.Concluimos que la conservación del polen a 4°C o a -18°C seríanlas más adecuadas, ya que permiten obtener una mayor concentraciónproteica partiendo de la misma masa de polen.
The active components from which pollen allergen extracts are obtainedcan change considerably according to the time or the placewhere collect and the time period between harvesting and use.This work aims to assess if the storage temperature of the pollengrain influences protein expression and its antigenicity when preparingan allergen extract. The species chosen for our study wasChenopodium album L, since it is of great allergologic interest inthe city of Bahía Blanca.Pollen grains were stored at room temperature 4ºC and -18ºC ,for a period of two months. The protein content of the extractswas determined by the Bradford method. Protein expressionand antigenicity were studied by vertical electrophoresis TricineSDS-PAGE 12, 5% and Immunoblot. The obtained results show that the total protein concentrationwas lower in the extracts of pollen stored at room temperaturethan in those under two conditions. Protein expression differsquantitatively in all extracts and even if the qualitative expressionis kept practically the same, in the Tricine SDS-PAGE geland the pollen stored at room temperature there appear a bandof MW inferior to 12 kDa. This band could result from the proteindegradation experienced by pollen stored at that temperature.As regards extract antigenicity, there are no qualitative differenceseven though there are significant quantitative differences.We conclude that pollen preservation at 4ºC or -18ºC would bethe most appropriate since it allows greater protein concentrationfor the same mass of pollen.
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Humans , Argentina , Allergens/immunology , Antigens, Plant/administration & dosage , Antigens, Plant/immunology , Pollen , TemperatureABSTRACT
Com o objetivo de avaliar a qualidade das amostras de leite conservadas nos silos de estocagem de duas indústrias de laticínios, foram coletadas sete amostras da indústria A e seis da indústria B. As amostras foram analisadas quanto aos parâmetros CCS, CBT, composição centesimal, contagem de microrganismos psicrotróficos e acidez titulável. A comparação de resultados entre os tipos de amostra foi realizada por meio do teste F da análise de variância. As análises estatísticas foram feitas por meio do programa de software SISVAR. Foram encontradas más condições de higiene dos utensílios e equipamentos usados nos silos; a temperatura e o tempo de estocagem estavam acima dos respectivos limites máximos permitidos pela legislação. Os resultados obtidos indicaram que as autoridades pertinentes não tem monitorado a qualidade do leite cru refrigerado recebido pelas indústrias de laticínios.
The present study analyzes the milk samples collected from the storing silos of two dairy industries,being seven samples from industry A and six from industry B. The SCC, TBC, centesimal composition,psychrotrophic microorganism counting and the titratable acidity were investigated. The results on typesof milk samples were statistically compared by means of test F of the variance analysis, employing theSISVAR software. Unsuitable hygienic conditions in appliances and equipments were found, and the milkstorage time-period and temperature were found to be over the respective maximum limits established by the legislation in force. Inadequate procedures in storing raw milk samples produce hazards that must bemitigated by monitoring the quality of products.
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Quality Control , Hygiene , Dairying , MilkABSTRACT
PURPOSE: To evaluate corneal endothelial cell changes in Optisol-GS(R) according to enucleation time at different storage temperatures after death. METHODS: Eight rabbit cadavers (16 eyes) were stored at -3 degrees C and room temperature, and enucleation was performed 10 and 24 hours postmortem. The samples were divided into four groups (Group 1 was -3 degrees C, 10 hours, Group 2 was room temperature, 10 hours, Group 3 was -3 degrees C, 24 hours, and Group 4 was room temperature, 24 hours). The corneas were stored in Optisol-GS(R) at 4 degrees C, and we measured corneal endothelial cell density and thickness by specular microscopy on days 1, 3, 5, 7, 10, and 14 of preservation. RESULTS: The densities and thicknesses of corneal endothelial cells of each of the four groups after enucleation showed no significant difference. Corneal endothelial cell density acceptable for penetrating keratoplasty (CD>2500 cells/mm2) was found in groups 1 and 3 until 14 days, in group 2 until 10 days, and in group 4 until 7 days. In particular, eyes stored at -3 degrees C had less corneal endothelial cell loss than at room temperature after 7 days and 14 days (P<0.05). CONCLUSIONS: This study demonstrated that when rabbit cadavers were stored at -3 degrees C, corneas could be preserved in Optisol-GS(R) for 14 days, even if the eyeballs from which they were prepared were extracted within 24 hours postmortem. Within 24 hours postmortem, the storing temperature of the cadavers was found to be more important than the enucleation time for the survival of corneal endothelial cells.
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Cadaver , Cornea , Corneal Endothelial Cell Loss , Endothelial Cells , Endothelium, Corneal , Eye , Keratoplasty, Penetrating , MicroscopyABSTRACT
BACKGROUND: Rocuronium bromide is a monoquaternary amino steroidal muscle relaxant. Rocuronium is structurally stable and no metabolites of rocuronium have not been observed in humans. The manufacturer recommends that rocuronium can be stored in room temperature for 12 weeks. The aim of this study was to determine if the storage temperature of rocuronium could influence the pharmacodynamics of rocuronium. METHODS: One hundred of patients with a class I or II ASA physical status were enrolled in this study. It was divided to two groups. One (Group '0', n = 50) consists of those who had intravenously administered the rocuronium which had been stored in refrigerator and the other (Group '14', n = 50) consists of those who had intravenously administered the rocuronium which had been stored in room temperature (20-29degrees C, median 25.1degrees C) for 14 days. Before an anesthesia was induced, TOF-Watch(R) was attached and calibrated. The anesthesia was induced with 1microgram/kg of fentanyl and 1.5 mg/kg of propofol intravenously. While the 0.1 Hz of single twitch was applied, 0.45 mg/kg of rocuronium, which is appointed to each group, was injected. Intubation is performed 90 seconds after injection of rocuronium and evaluated the intubating condition as excellent, good, poor, and impossible. RESULTS: There was a statistically significant difference in intubating condition at 90 seconds between two groups. The onset time to twitch depression of 0% in group '14' was prolonged compared to group '0' (P < 0.05). Clinical duration was also shortened in group '14' (P < 0.05). CONCLUSIONS: Compared with the use of rocuronium stored in refrigerator, that stored at room temperature can be expected to have unfavorable intubating condition at 90 seconds after rocuronium injection. Therefore, the storage temperature has some influences on the efficacy of rocuronium.
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Humans , Anesthesia , Depression , Fentanyl , Intubation , PropofolABSTRACT
OBJECTIVE: To investigate and analyze the storage temperatures of drugs for references of drug storage. METHODS: A classified statistical analysis was conducted on those drugs with temperature requirements in storage as instructed in drug package inserts. RESULTS: The stock drugs totaled 1 254 kinds,of which,483 (38.52%) had the item of temperature requirements in storage,158 with room temperature storage and 61 with cold storage had the item of specific temperature requirement. CONCLUSION: The storage temperature of drugs should be established based on the quality of different drugs so as to ensure the stability of drug quality. It is advisable to clarify the storage temperature in all the drug package inserts.
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BACKGROUND: FDA recommend that botulinum toxin should be used within 4 hours after reconstruction. Because botulinum toxin is very expensive and also only small amounts of botulinum toxin are needed for one lesion, it should be used for several patients simultaneously to reduce cost. The reports on the decrease of potency according to storage temperature and duration were contradictory among the investigators. OBJECTIVE: The purpose of this study is to compare the change of the potency in various storage temperatures and duration and, to determine the optimal conditions for storage of botulinum toxin without potency reduction. METHODS: The potency of botulinum toxin was measured by the reduction rate of tension of the injected gastrocnemius muscle of Sprague-Dawley rats. The potency of botulinum toxin could be estimated through the comparison of the reduction rate of tension between two muscles; botulinum toxin injected muscle and normal saline injected control muscle, which was denoted as % paralysis. RESULTS: Botulinum toxin induced muscle paralysis in a dose-dependent manner. Muscle was paralysed by 9.8+/-0.6(mean+/-standard error), 10.2+/-2.7, 38.3+/-13.6, and 93.7+/-0.5% at 0(injected normal saline to both sides of gastrocnemius muscles of the same rat), 0.01, 0.1, and 1unit/0.1ml of fresh botulinum toxin injection, respectively. Percent paralyses by 1unit/0.1ml of stored botulinum toxin at 4degreeC and -20degreeC were 98.8+/-0.6% and 98.2+/-0.9% in 4 weeks, respectively. Percent paralyses by 0.1 unit/0.1 ml of stored botulinum toxin at 4degreeC and -20degreeC were 29.6+/-4.8% and 35.5+/-15.1% in 4 weeks, respectively. CONCLUSION: With these findings, the authors proved that if botulinum toxin is stored in refrigerator(4degreeC) or refreezer(-20degreeC) after reconstruction, it can be used without the decrease of its potency.