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蘇州艾特森制藥設(shè)備有限公司
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蘇州艾特森制藥設(shè)備有限公司
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更新時(shí)間：2023-07-21 13:11:41瀏覽次數(shù)：156次
聯(lián)系我時(shí)，請(qǐng)告知來自 化工機(jī)械設(shè)備網(wǎng)蘇州艾特森制藥設(shè)備有限公司主營脂質(zhì)體擠出器,臺(tái)式脂質(zhì)體擠出器,微流控,微流控芯片,LNP微流控,mRNA微流控,實(shí)驗(yàn)型旋轉(zhuǎn)滅菌柜,SiRNA脂質(zhì)體,mRNA脂質(zhì)體,陽離子脂質(zhì)體,脂質(zhì)體制備,疫苗脂質(zhì)體,疫苗脂質(zhì)體,核酸脂質(zhì)體,擠出儀,雙螺桿熱熔擠出機(jī),立式滅菌柜,高壓均質(zhì)機(jī),剪切機(jī),公司位于蘇州工業(yè)園區(qū),是一家自主研發(fā)、專業(yè)生產(chǎn)及銷售制藥裝備的科技生產(chǎn)型企業(yè)!
TLEx 罐體式脂質(zhì)體擠出器
TLEx Tank Liposome Extruder
主要應(yīng)用
◆脂質(zhì)體 Doxorubicin liposome
◆ 脂質(zhì)體 Amphotericin B liposome
◆ 脂質(zhì)體 Paclitaxel liposomes
◆ 脂質(zhì)體 Oxaliplatin liposomes
◆ 伊立替康脂質(zhì)體 Irinotecan liposome
◆ SiRNA 脂質(zhì)體 SiRNA liposome
◆ 白蛋白納米粒 Albumin paclitaxel nanoparticles
◆ 核酸類脂質(zhì)體 Nucleic acid liposome
◆ mRNA脂質(zhì)體 mRNA liposome
擠出原理
Extrusion Principle
擠出原理圖
Extrusion schematic diagram
◆樣品經(jīng)過水化形成脂質(zhì)體后，一般會(huì)通過高壓均質(zhì)或者超聲的方式對(duì)樣品進(jìn)行初步均質(zhì)處理，處理后樣品粒徑和分布都會(huì)有所提高，但往往還不能達(dá)到所需要的理想要求。此時(shí)，將均質(zhì)后樣品由下圖中進(jìn)料口進(jìn)入，通過高壓氮?dú)鈱悠窂臑V膜中擠出，擠出后的樣品粒徑和分布都會(huì)進(jìn)一步提高。
After the sample is hydrated to form liposomes, the sample is usually homogenized by high-pressure homogenization or ultrasonic wave. After treatment, the particle size and distribution of the sample will be improved, but it can not meet the desired requirements. At this time, the homogenized sample enters through the feed port in the figure below, and the sample is extruded from the filter membrane by high-pressure nitrogen. The particle size and distribution of the extruded sample will be further improved
支撐板
Support plate
◆支撐板和濾板主要起到支撐濾膜的作用。 由于磷脂有一定的相變溫度，所以在擠出之前需要對(duì)擠出器夾套通入恒溫水進(jìn)行預(yù)熱至一定溫度（如70℃），且在使用過程中需保持在此溫度。通常的脂質(zhì)體品種擠出之后粒徑能達(dá)到 100nm以下，PDI 能控制在 0.1 以下。
The supporting plate and filter plate mainly play the role of supporting the filter membrane. Since the phospholipid has a certain phase transition temperature, it is necessary to preheat the extruder jacket with constant temperature water before extrusion to a certain temperature (such as 70 ℃), which should be maintained in the process of use. After extrusion, the particle size of liposomes can reach below 100nm and PDI can be controlled below 0.1.
◆動(dòng)力源：氮?dú)?/span>
Power source: nitrogen
技術(shù)特征
Technical features
◆核心部件 The core components
支撐板（SS316L不銹鋼）
Support plate (SS316L stainless steel)
濾板（SS316L不銹鋼）
Filter plate (SS316L stainless steel)
濾膜:PC材質(zhì)（聚碳酸酯）
Filter membrane :PC material (polycarbonate)
密封系統(tǒng)：PU材質(zhì)/聚四氟乙烯
Sealing system: PU material/polytetrafluoroethylene
溫控系統(tǒng)：夾套控溫
Temperature control system: jacket temperature control
◆技術(shù)特點(diǎn) Technical characteristics
所有部件包括“O"型圈，墊圈均通過FDA 認(rèn)證
All parts including "O" rings, gaskets are FDA approved
操作便捷，可重復(fù)使用
Easy to operate and reusable
嚴(yán)格控制產(chǎn)品粒徑，可單次操作或循環(huán)操作
Strictly control the particle size of products, single operation or cycle operation
裝卸方便，便于清洗和滅菌
Easy loading and unloading, easy cleaning and sterilization
所有數(shù)據(jù)可直接放大
All data can be directly amplified
預(yù)設(shè)壓力保護(hù)閥
Preset pressure protection valve
可用于高濃度樣品處理
Can be used for high concentration sample processing
可放在潔凈室中使用，符合 GMP 標(biāo)準(zhǔn)
Can be used in a clean room, accord with GMP standards
技術(shù)參數(shù)
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