31 results match your criteria: "Ltd. Research Center[Affiliation]"

Enhancing glioblastoma therapy via intranasal administration of highly potent cell-penetrating peptide decorated nanoparticles.

J Control Release

January 2025

Department of Global Innovative Drugs, The Graduate School of Chung-Ang University, 221 Heukseok-dong, Dongjak-gu, Seoul 06974, Republic of Korea; College of Pharmacy, Chung-Ang University, 221 Heukseok-dong, Dongjak-gu, Seoul 06974, Republic of Korea. Electronic address:

Glioblastoma multiforme (GBM) is a devastating primary tumor of the central nervous system with a significantly poor prognosis. The primary challenge in treating GBM lies in the restrictive nature of the blood-brain barrier (BBB), impeding effective drug delivery to the brain. In this study, intranasal polymeric micelles encapsulating a quercetin-etoposide combination were developed to induce synergistic apoptotic effects and enhance direct drug delivery to the brain.

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Atopic dermatitis is a chronic inflammatory skin condition that is characterized by skin inflammation, itching, and redness. Although various treatments can alleviate symptoms, they often come with side effects, highlighting the need for new treatments. Here, we discovered a new peptide-based therapy using the intra-dermal delivery technology (IDDT) platform developed by Remedi Co.

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Background/aim: This research investigated the biophysical properties, safety, and efficacy of polydioxanone (PDO) filler compared to poly-L-lactic acid (PLLA), polycaprolactone (PCL), and hyaluronic acid (HA) fillers. In both mouse and human skin models, a novel collagen stimulation was compared with hyaluronic acid filler.

Materials And Methods: An electron microscope was used to capture images of the solid particle microsphere shape.

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Respiratory virus infections are an escalating issue and have become common worldwide. Influenza and COVID-19 are typical infectious respiratory diseases, and they sometimes lead to various complications. In a situation in which no established drug or treatment exists, consumption of proper food might be beneficial in maintaining health against external infections.

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Novel extended IVIVC combined with DoE to predict pharmacokinetics from formulation compositions.

J Control Release

March 2022

College of Pharmacy, Wonkwang University, 460 Iksan-daero, Iksan, Jeonbuk 54538, Republic of Korea. Electronic address:

Article Synopsis
  • The study aimed to create a new extended in vitro in vivo correlation (IVIVC) model that combines design of experiments (DoE) to predict how sustained-release (SR) tablets behave in the body based on their formulation.
  • Nineteen different ketoprofen SR tablets were formulated and tested to establish mathematical relationships between their composition and dissolution profiles, achieving high accuracy in predictions.
  • The final model successfully connected the in vitro and in vivo pharmacokinetic data, demonstrating an average prediction error of less than 5%, allowing for effective predictions of drug behavior and optimizing future tablet formulations.
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Alleviative effects of Fara-darmani Consciousness Field on L. under salinity stress.

F1000Res

December 2020

Institute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, 13145-1384, Iran.

: The Fara-darmani Consciousness Field was founded by Mohammad Ali Taheri. It is a novel field and is described similarly to the field of gravity, or the electromagnetic field. This field is neither matter nor energy, and therefore does not possess a quantity.

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Acyclovir is a Biopharmaceutics Classification System (BCS) class III antiviral agent which is only absorbed in the upper part of the gastrointestinal tract. This study aimed to establish a new in vitro-in vivo correlation (IVIVC) platform based on population pharmacokinetic modeling for drugs with site-dependent absorption using acyclovir as a model drug. Three types of sustained-release (SR; 500 mg) acyclovir tablets were prepared by the wet granulation method.

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Gastroretentive (GR) systems are designed to prolong gastric residence time to allow sustained absorption and improve the oral bioavailability of drugs with a narrow absorption window in the upper part of the gastrointestinal tract. The present study aimed to develop a GR system for acyclovir using 3D printing technology and evaluate its in vivo pharmacokinetics after oral administration in Beagle dogs. The system consisted of a gastro-floating device, which can float in the gastric fluid, prepared by a fused deposition modeling 3D printer and conventional acyclovir sustained-release (SR) tablet.

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An oral toxicity test in rats and a genotoxicity study of extracts from the stems of Opuntia ficus-indica var. saboten.

BMC Complement Altern Med

January 2019

Department of Integrated Biomedical and Life Sciences, Graduate School, Korea University, Seoul, 02841, Republic of Korea.

Background: Opuntia ficus-indica var. saboten (OFIS) is used widely in Korea to treat constipation due to its diuretic effects and its enhancement of bowel function and appetite. However, its safety has not yet been established.

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In vitro-in vivo correlation (IVIVC), a predictive mathematical model between the in vitro dissolution and the in vivo pharmacokinetics has been utilized for the development of new extended release (ER) formulations. The aim of the present study was to extend the IVIVC approach, which correlates among the formulation composition, the in vitro dissolution, and the plasma drug concentration, to predict plasma drug concentrations from a given composition of the formulation, and vice versa, using baclofen as a model drug. Baclofen ER tablets with different dissolution rates were prepared by varying the composition of hydroxypropyl methylcellulose (HPMC).

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Background: Human skin aging is caused by several factors, such as UV irradiation, stress, hormone, and pollution. Wrinkle formation and skin pigmentation are representative features of skin aging. Although EGF and arbutin are used as anti-wrinkle and skin whitening agents, respectively, they have adverse effects on skin.

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Etanercept is a dimeric genetic recombinant glycoprotein consisting of Fc domain of human Immunoglobulin G1 and the extracellular domain of human tumor necrosis factor (TNF) receptor type II. Etanercept exerts therapeutic effects on inflammatory diseases such as rheumatoid arthritis and juvenile idiopathic arthritis by neutralizing biological activities of TNFα/Lymphotoxin (LT) α. Mochida Pharmaceutical and LG Chem have developed syringe, pen, and vial products of Etanercept BS (biosimilar) as the first biosimilar of Enbrel in Japan.

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Epidemiology, clinical characteristics, and risk factors for mortality of early- and late-onset invasive candidiasis in intensive care units in China.

Medicine (Baltimore)

October 2017

Nanjing Zhongda Hospital, Southeastern University School of Medicine, Nanjing West China Hospital of Sichuan University, Chengdu Shengjing Hospital of China Medical University, Shenyang The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou Henan Provincial People's Hospital, Zhengzhou Tianjin Third Central Hospital, Tianjin The First Affiliated Hospital of Medical School of Zhejiang University, Hangzhou Guangdong General Hospital, Guangzhou Daping Hospital, Chongqing MSD (China) Holding Co., Ltd. Research Center for Medical Mycology, Peking University First Hospital, Peking University, Beijing, China.

To identify the epidemiology, treatments, outcomes, and risk factors for patients with early- or late-onset invasive candidiasis (EOIC or LOIC) in intensive care units in China.Patients were classified as EOIC (≤10 days) or LOIC (>10 days) according to the time from hospital admission to IC onset to identify distinct clinical characteristics.There were 105 EOIC cases and 201 LOIC cases in this study.

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Introduction: The objective was to investigate the effects of melatonin and exercise on insulin resistance (IR), hypertension and fatigue syndrome in a rat model of type 2 diabetes mellitus (T2DM).

Materials And Methods: Rats were divided into 5 groups namely normal control (NC), T2DM control group (DC), diabetes plus exercise (DE), diabetes plus oral melatonin supplement (DM) and diabetes plus melatonin and exercise (DME) groups. Melatonin was administered orally 5mg/kg twice daily and 40min swimming/day 5days/week were regimented after diabetes induction.

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Cosmeceutical product consisting of biomimetic peptides: antiaging effects in vivo and in vitro.

Clin Cosmet Investig Dermatol

January 2017

Department of Pathomorphology, D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology, Saint-Petersburg, Russian Federation.

Background: Biomimetic peptides are synthetic compounds that are identical to amino acid sequence synthesized by an organism and can interact with growth factor receptors and provide antiaging clinical effects.

Purpose: The purpose of this study was to investigate the effects of biomimetic peptides on the repair processes in the dermis using a model of cell cultures and in vivo.

Patients And Methods: Five female volunteers were subjected to the injection of biomimetic peptides 1 month prior to the abdominoplasty procedure.

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Highly ytterbium-doped bismuth-oxide-based fiber.

Opt Express

August 2009

Asahi Glass Co, Ltd Research Center, Yokohama 221-8755, Japan.

Thermally stable highly ytterbium-doped bismuth-oxide-based glasses have been investigated. The absorbance increased linearly with Yb(2)O(3) concentration, reaching 7800 dB/m with 3 mol-% of Yb(2)O(3). An ytterbium-doped bismuth-oxide-based fiber has also been fabricated with a fiber loss of 0.

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We have fabricated BaO-TiO2-GeO2-SiO2-based glass fibers with the oriented space-selectively crystallized structure by laser irradiation and also demonstrated variable optical attenuation induced by electro-optical birefringence change based on second-order optical nonlinearity. The transmittance of a polarized signal is controlled by an electric field applied to the fiber, and the electro-optic fiber devices are operated with extremely low nanowatt electric power dissipation.

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Separation of complex mixtures of fluorobenzoic acids by capillary electrophoresis.

J Sep Sci

February 2009

Analytical Science & TechnologyFunction, Asahi Glass Co., Ltd.Research Center, Yokohama,Kanagawa, Japan.

Fluorobenzoic acids are important intermediates in the synthesis of antibacterial drugs. Conditions for the separation of mixtures of twenty-five acids by CE have been optimized. A set of conditions with phosphate buffer (pH 3.

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Achromatic polarization rotator.

Appl Opt

September 2007

Samsung Electronics Company, Ltd. Research Center, 29, 1-st Brestskaya Street, Moscow 125047, Russia.

What we believe to be a new optical element consisting of a single piece isotropic material with three internally reflecting faces for polarization plane rotation by the angle phi=pi/2 is proposed. The principle of operation is based on the geometrical phase effect, which is different in its origin but produces a similar effect to the circular birefringence. It is shown that the rotator made of polymer as well as silica glasses is not affected by the chromatic dispersion in a visible range.

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Background: Prevention of Type 1 diabetes mellitus (T1DM), a major childhood chronic disease with rapidly increasing incidence, is an urgent topic of research. We investigated whether 5% oligofructose (OF) as compared to 5% cellulose had a protective effect against diet-induced T1DM in the diabetes-prone BioBreeding (BB) rat model.

Methods: Groups of BB rats were fed the experimental diets from weaning.

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The potential benefits of SM-20302, (2S)-3-(3-(4-amidinobenzoylamino)propanoylamino)-2-(4-ethyl)benzensulfonylaminopropionic acid hydrochloride, a nonpeptide GPIIb/IIIa receptor antagonist, were compared with those of aspirin and ticlopidine in a transient cerebral ischemia model in guinea pigs. Transient cerebral ischemia was induced in guinea pigs by an infusion of ADP/epinephrine into the left internal carotid artery. Each compound was orally administered 1 h (SM-20302 and aspirin) or 3 h (ticlopidine) before the ADP/epinephrine infusion.

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We have developed a gastrointestinal hemorrhage model in mice and thereby assessed the potential risk of bleeding following administration of SM-20302, a nonpeptide GPIIb/IIIa receptor antagonist. First, SM-20302 selectively inhibited the interaction between human platelets and fibrinogen in vitro. Second, SM-20302 dose-dependently inhibited ADP-induced ex vivo platelet aggregation in mice and produced an ED50 value of 0.

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SM-20302, a synthetic inhibitor of the fibrinogen receptor of platelets, has been shown to inhibit the platelet aggregation induced by various stimuli. In the present study, we performed ex vivo platelet aggregation studies by using heparinized platelet-rich plasma (PRP) as well as citrated PRP and compared the antiaggregatory activity with the in vivo antithrombotic efficacy of SM-20302. The oral administration of SM-20302 (0.

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Background: Oral administration of an antigen has been shown to suppress the specific immune response to this antigen. This approach, called oral tolerance, has been demonstrated with intact proteins in animal models for prevention of allergy and autoimmune diseases.

Objective: The purpose of this study was to determine whether oral tolerance can be induced with protein peptides.

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Osteoporosis as a pediatric problem.

Pediatr Clin North Am

August 1995

Department of Nutrition, Nestec Ltd. Research Center, Lausanne, Switzerland.

Osteoporosis has long been considered a disease of the elderly; however, there is now a general agreement that predisposition begins in childhood and adolescence; thus, rational approaches to prevention of the disease should be started during childhood and adolescence. Indeed, by determining PBM, events occurring in the first two decades of life may determine in large part the subsequent risk of osteoporosis. Attention has thus been focused on the physiology of bone mass accumulation during growth, including the role of environmental factors such as dietary calcium and exercise.

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