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Featured researches published by Takakuni Matsuda.


Biological & Pharmaceutical Bulletin | 2017

Preparation of an Ultrafine Rebamipide Ophthalmic Suspension with High Transparency

Takakuni Matsuda; Shogo Hiraoka; Hiroki Urashima; Ako Ogura; Tatsuhiro Ishida

A 2% commercially available, milky-white, rebamipide micro-particle suspension is used to treat dry eyes, and it causes short-term blurring of the patients vision. In the current study, to improve the transparency of a rebamipide suspension, we attempted to obtain a clear rebamipide suspension by transforming the rebamipide particles to an ultrafine state. In the initial few efforts, various rebamipide suspensions were prepared using a neutralizing crystallization method with additives, but the suspensions retained their opaque quality. However, as a consequence of several critical improvements in the neutralizing crystallization methods such as selection of additives for crystallization, process parameters during crystallization, the dispersion method, and dialysis, we obtained an ultrafine rebamipide suspension (2%) that was highly transparent (transmittance at 640 nm: 59%). The particle size and transparency demonstrated the fewest level of changes at 25°C after 3 years, compared to initial levels. During that period, no obvious particle sedimentation was observed. The administration of this ultrafine rebamipide suspension (2%) increased the conjunctival mucin, which was comparable to the commercially available micro-particle suspension (2%). The corneal and conjunctival concentration of rebamipide following ocular administration of the ultrafine suspension was slightly higher than that of the micro-particle suspension. The ultrafine rebamipide suspension (eye-drop formulation) with a highly transparent ophthalmic clearness should improve a patients QOL by preventing even a shortened period of blurred vision.


Cancer Research | 2013

Abstract 4430: Protective effects of rebamipide liquid on radiation-induced glositis in rats.

Takako Nakashima; Naoya Uematsu; Masafumi Shibamori; Kazushi Sakurai; Masayuki Sato; Takakuni Matsuda; Nobutomo Sako

Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC [Background & Aims] Rebamipide is widely used for mucosal protection, healing of gastric ulcers and treatment of gastritis. Recently, it was reported that Rebamipide gargle inhibited oral mucositis induced by chemoradiotherapy in head and neck cancer patients. In this study, we examined protective effects of Rebamipide Liquid on radiation-induced glossitis rat model and analyzed the expression level of pro-inflammatory cytokines and chemokines in the injury area of tongue. [Materials & Methods] Rebamipide Liquid, comprising with Rebamipide crystals less than 500 nm particles, was prepared by a neutralizing crystallization technique. This formulation is a stable homogenous aqueous suspension provided with appropriate viscosity by adding viscosity enhanced agents to improve the retention in the oral cavity. The glossitis was induced by X-ray with 15Gy irradiation only around the snout (Day 0) in rats. Rebamipide Liquid was administered intraorally at doses of 5, 10 or 20 mg/kg (1, 2 or 4%, respectively), 6 times a day for 14 days from Day -7 to Day 6. These tongue tissue specimens were obtained at Day 7 and their images were recorded by a digital camera for efficacy evaluations. Gene expression analysis was performed with quantitative real-time PCR (ABI) and protein level was evaluated with Bio-Plex system(BioRad) or ELISA in a different study which was conducted at the two doses of 0 and 20 mg/kg (0 and 4%). [Result & Conclusions] The ulcer-like areas (10.8 ± 1.2, 7.9 ± 1.1 and 7.0 ± 0.7%) at doses of 5 - 20 mg/kg (1 - 4%) of Rebamipide Liquid administration, were statistically smaller than the vehicle control at 14.7±1.6%. Another study revealed that the expression of pro-inflammatory cytokines (TNF-α, IL-6 and Il-1β) and chemokines (MCP-1 and Gro-α) were dramatically elevated in the irradiated tongue at Day7, as compared to normal. But these elevated expressions were significantly suppressed by the 4% Rebamipide treatment. These immuoassays elucidated that the production of these cytokines and chemokines were significantly suppressed by the Rebamipide administration. These results demonstrated that the Rebamipide Liquid has a potent pharmacological action for the radiation-induced oral mucositis mediated by the suppression of pro-inflammatory cytokines (TNF-α, IL-6 and Il-1β) and chemokines (MCP-1 and Gro-α). Citation Format: Takako Nakashima, Naoya Uematsu, Masafumi Shibamori, Kazushi Sakurai, Masayuki Sato, Takakuni Matsuda, Nobutomo Sako. Protective effects of rebamipide liquid on radiation-induced glositis in rats. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 4430. doi:10.1158/1538-7445.AM2013-4430


Archive | 2004

Controlled release sterile injectable aripiprazole formulation and method

Janusz W. Kostanski; Takakuni Matsuda; Manoj Nerurkar; Vijay H. Naringrekar


Archive | 2003

Package for medical fluid

Yoshito Masuda; Takakuni Matsuda


Archive | 2008

Methods for producing aripiprazole suspension and freeze-dried formulation

Shogo Hiraoka; Takakuni Matsuda; Junichi Hatanaka


Archive | 2005

Aqueous ophthalmic suspension of crystalline rebamipide

Takakuni Matsuda; Shogo Hiraoka; Yuso Tomohira; Shinichi Ishikawa


Archive | 2008

Benzazepine derivatives useful as vasopressin antagonists

Kazumi Kondo; Yasuhiro Menjo; Takahiro Tomoyasu; Shin Miyamura; Yuso Tomohira; Takakuni Matsuda; Keigo Yamada; Yusuke Kato


Archive | 2007

Hydrogel Suspension and Manufacturing Process Thereof

Shogo Hiraoka; Takakuni Matsuda


Biological & Pharmaceutical Bulletin | 2014

Novel Submicronized Rebamipide Liquid with Moderate Viscosity: Significant Effects on Oral Mucositis in Animal Models

Takako Nakashima; Nobutomo Sako; Takakuni Matsuda; Naoya Uematsu; Kazushi Sakurai; Tatsuhiro Ishida


Archive | 1996

PACKAGE HOLDING A PROCATEROL HYDROCHLORIDE AQUEOUS SOLUTION FORMULATION, AND A PROCATEROL HYDROCHLORIDE AQUEOUS SOLUTION FORMULATION

Yuzo Kimura; Shinichi Ishikawa; Masafumi Toda; Takakuni Matsuda

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