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1.
AAPS PharmSciTech ; 25(4): 81, 2024 Apr 10.
Article in English | MEDLINE | ID: mdl-38600252

ABSTRACT

MALCORE®, a novel manufacturing technology for drug-containing particles (DCPs), relies on the melt granulation method to produce spherical particles with high drug content. The crucial aspect of particle preparation through MALCORE® involves utilizing polymers that dissolve in the melt component, thereby enhancing viscosity upon heating. However, only aminoalkyl methacrylate copolymer E (AMCE) has been previously utilized. Therefore, this study aims to discover other polymers and comprehend the essential properties these polymers need to possess. The results showed that polyvinylpyrrolidone (PVP) was soluble in the stearic acid (SA) melt component. FTIR examination revealed no interaction between SA and polymer. The phase diagram was used to analyze the state of the SA and polymer mixture during heating. It revealed the mixing ratio and temperature range where the mixture remained in a liquid state. The viscosity of the mixture depended on the quantity and molecular weight of the polymer dissolved in SA. Furthermore, the DCPs prepared using PVP via MALCORE® exhibited similar pharmaceutical properties to those prepared with AMCE. In conclusion, understanding the properties required for polymers in the melt granulation process of MALCORE® allows for the optimization of manufacturing conditions, such as temperature and mixing ratios, for efficient and consistent drug layering.


Subject(s)
Polymers , Povidone , Technology, Pharmaceutical/methods , Temperature , Excipients , Technology , Methacrylates , Drug Compounding/methods , Solubility
2.
Oral Maxillofac Surg ; 24(3): 289-298, 2020 Sep.
Article in English | MEDLINE | ID: mdl-32342247

ABSTRACT

OBJECTIVE: We aimed to investigate the usefulness of glucose administration for maintaining perioperative glycemic control in patients with dietary restrictions during 4 h prior to impacted mandibular third molar extraction under intravenous sedation. METHODS: Fifty-four individuals scheduled to undergo extraction of impacted mandibular third molars under intravenous sedation, with preoperative blood glucose levels (GL) of 70-110 mg/dL, were evaluated and divided into 3 groups (n = 18 each): control group receiving glucose-free sodium lactate Ringer's solution, perioperative GL group receiving 100 mL of 5% glucose solution immediately after local anesthesia, and postoperative GL group receiving 100 mL of 5% glucose solution immediately after surgery completion. Blood glucose levels, systolic blood pressure, diastolic blood pressure, and heart rate were measured. RESULTS: Glucose levels of those in the control and perioperative GL groups decreased within the standard range 90 min after surgery, compared with the preoperative blood glucose level. However, in the postoperative GL group, glucose levels were similar to the preoperative levels. Systolic and diastolic blood pressure and heart rate were not affected by glucose administration, and sedation could be maintained without an invasive procedure. CONCLUSIONS: Following a restriction on eating and drinking 4 h prior to surgery, the blood glucose level gradually decreased in the perioperative period but remained within the reference range until 90 min following surgery. The administration of 100 mL 5% glucose solution immediately after surgery was sufficient for the prevention of postoperative hypoglycemia. This approach may be useful for perioperative glycemic control during third molar extraction.


Subject(s)
Blood Glucose , Tooth, Impacted , Glucose , Humans , Mandible , Molar, Third , Tooth Extraction
3.
Genes Cells ; 18(5): 410-24, 2013 May.
Article in English | MEDLINE | ID: mdl-23506116

ABSTRACT

Reelin-Dab1 signaling is indispensable for proper positioning of neurons in mammalian brain. Reelin is a glycoprotein secreted from Cajal-Reztuis cells in marginal zone of cerebral cortex, and its receptors are Apolipoprotein E receptor 2 (ApoER2) or very low density lipoprotein receptor (VLDLR) expressed on migrating neurons. When Reelin binds to ApoER2 or VLDLR, an adaptor protein Dab1 bound to the receptors undergoes Tyr phosphorylation that is essential for Reelin signaling. We reported previously that Cdk5-p35 phosphorylates Dab1 at Ser400 and Ser491 and the phosphorylation regulates its binding to CIN85, which is an SH3-containing multiadaptor protein involved in endocytic downregulation of receptor-tyrosine kinases. However, the interaction of CIN85 with Dab1 has not been addressed in neurons. We examined here a possibility that CIN85 has a role in Reelin signaling. We found nonpho-sphorylated Dab1-mediated colocalization of CIN85 with ApoER2. The colocalization of CIN85 with ApoER2 was increased in neurons stimulated with Reelin repeats 3-6, an active Reelin fragment. The stimulation recruited CIN85 to domains in plasma membrane where it colocalized with ApoER2 and Dab1 and then to EEA1-labeled early endosomes in the cytoplasm. In addition, Tyr phosphorylation of Dab1 strengthened the binding to CIN85. These results suggest that CIN85 participates in Reelin signaling through the binding to Dab1.


Subject(s)
LDL-Receptor Related Proteins/metabolism , Neoplasm Proteins/metabolism , Nerve Tissue Proteins/metabolism , Neurons/metabolism , Receptors, Cell Surface/metabolism , Receptors, LDL/metabolism , Adaptor Proteins, Signal Transducing , Animals , COS Cells , Cell Adhesion Molecules, Neuronal/chemistry , Cerebral Cortex/cytology , Chlorocebus aethiops , Endocytosis , Endosomes/metabolism , Extracellular Matrix Proteins/chemistry , HEK293 Cells , Humans , Mice , Nerve Tissue Proteins/chemistry , Neurons/cytology , Phosphorylation , Phosphotyrosine/metabolism , Protein Binding , Protein Transport , Proto-Oncogene Proteins c-fyn/metabolism , Reelin Protein , Serine Endopeptidases/chemistry , Subcellular Fractions/metabolism
4.
J Insect Physiol ; 56(9): 1022-31, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20206631

ABSTRACT

Butterfly wing color patterns can be modified by the application of temperature shock to pupae immediately after pupation, which has been attributed to a cold-shock-induced humoral factor called cold-shock hormone (CSH). Here, we physiologically characterized CSH and pharmacological action of tungstate, using a nymphalid butterfly Junonia orithya. We first showed that the precise patterns of modification were dependent on the time-point of the cold-shock treatment after pupation, and confirmed that the modification properties induced in a cold-shocked pupa were able to be transferred to another pupa in a parabiosis experiment. Cold-shock application after removal of the head and prothorax together still produced modified wings, excluding major involvement of the brain-retrocerebral neuroendocrine complex. Furthermore, tungstate injection induced modifications even in individuals whose head and prothorax were removed. Importantly, transplantation of tracheae isolated from cold-shocked pupae induced modifications in the recipient wings. We identified a chemical peak in hemolymph of the cold-shocked individuals using HPLC, which corresponded to dopamine, and demonstrated that dopamine and its related biogenic amines have ability to induce small color-pattern changes. Taken together, the present study suggests that CSH is likely to be secreted from trachea-associated endocrine cells upon cold-shock treatment and that tungstate may change color patterns via its direct action on wings.


Subject(s)
Butterflies/physiology , Cold Temperature , Insect Hormones/metabolism , Pigmentation/physiology , Stress, Physiological , Wings, Animal/physiology , Animals , Chromatography, High Pressure Liquid , Dimethyl Sulfoxide , Dopamine/metabolism , Endocrine Cells/metabolism , Hemolymph/chemistry , Pigmentation/drug effects , Pupa/anatomy & histology , Pupa/physiology , Time Factors , Trachea/cytology , Tungsten Compounds/pharmacology , Wings, Animal/drug effects
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