产品
编 号：F081435
分子式：C43H79NO2
分子量：642.09
分子式：C43H79NO2
分子量：642.09
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
询价
询价
5mg
询价
询价
10mg
询价
询价
25mg
询价
询价
50mg
询价
询价
100mg
询价
询价
结构图
CAS No: 1224606-06-7
产品详情
生物活性：
D-Lin-MC3-DMA, an ionizable cationic lipid, is a potent siRNA delivery vehicle.
体内研究：
含有二硬脂酰磷脂酰胆碱 (DSPC) 的脂质纳米颗粒 (LNP) 和可电离的氨基脂质，例如二亚油基甲基-4-二甲基氨基丁酸酯 (DLin-MC3-DMA) 是有效的体内 siRNA 运载工具。LNP-siRNA 系统经过优化以在小鼠静脉注射后的肝细胞中实现最大基因沉默效力，其中包含摩尔比为 50/10/38.5/1.5 的 DLin-MC3-DMA (MC3)、DSPC、胆固醇和聚乙二醇 (PEG)-脂质。DLin-MC3-DMA 具有优化的 pKa 值，可显著增强效力。
体外研究：
Preparation of MC3 Lipid NanoparticlesHere we provide lipid molar ratios for LNPs in FDA-approved Patisiran (a siRNA targets the transthyretin (TTR) mRNA). The molar ratio of lipids in this formulation is D-Lin-MC3-DMA : DSPC : Cholesterol : PEG2000-C-DMG = 50 : 10 : 38.5 : 1.5, and RNA to lipid weight ratio is 0.05 (wt/wt). A. Lipid Mixture Preparation1. Dissolve lipids in ethanol and prepare 10 mg/m stock solutions. The lipid stock solutions can be stored at ?20°C for later use.Note 1:The ionizable lipid is usually a liquid. Due to the viscosity, it should always be weighed rather than relying on the autopipette volume. Note 2: Cholesterol in solution should be kept warm (>37℃) to maintain fluidity. Transfer the cholesterol solution promptly to avoid cooling. 2. Prepare the lipid mixture solution as described. For each mL of lipid mixture add the following: 548 μL of 10mg/mL D-Lin-MC3-DMA (HY-112251), 254 μL of 10mg/mL Cholesterol (HY-N0322), 134 μL of 10mg/mL DSPC (HY-W040193), and 64 μL of PEG2000-C-DMG (HY-145411) . Mix the solutions thoroμghly to achieve a clear solution. This mixture contains 10 mg of total lipid. Note 3: The choice of lipids and ratios may be changed as desired and this will affect the LNP properties (size, polydispersity, and efficacy) and the amount of mRNA required. B. siRNA Preparation1. Prepare a 166.7 μg/mL siRNA solution with 100 mM pH 5 sodium acetate buffer. Note 4: The lipid:siRNA weight ratio influences the encapsulation efficiency. Other weight ratios may be prepared as alternative formulations and should be adjusted accordingly by user.C. MixingThere are three commonly used methods to achieve rapid mixing of the solutions: the pipette mixing method, the vortex mixing method, and the microfluidic mixing method. All these mixing methods can be used for various applications. It is important to note that pipette mixing method and vortex mixing method may yield more heterogeneous LNPs with lower encapsulation efficiencies and is prone to variability. Microfluidic devices enable rapid mixing in a highly controllable, reproducible manner that achieves homogeneous LNPs and high encapsulation efficiency. Within these devices, the ethanolic lipid mixture and aqueous solution are rapidly combined in individual streams. LNPs are formed as the two streams mix and are then collected into a single collection tube. 1. Pipette Mixing Method: 1.1. Pipette 3 mL of the siRNA solution and quickly add it into 1 mL of the lipid mixture solution (A 1:3 ratio of ethanolic lipid mixture to aqueous buffer is generally used.) Pipette up and down rapidly for 20–30 seconds. 1.2. Incubate the resulting solution at room temperature for up to 15 minutes. 1.3. After mixing, the LNPs were dialyzed against PBS (pH 7.4) for 2 h, sterile filtered using 0.2 μm filters, and stored at 4°C. 2. Vortex Mixing Method: 1.1. Vortex 3 mL of siRNA solution at a moderate speed on the vortex mixer. Then, Quickly add 1 mL of the lipid mixture solution into the vortexing solution (A 1:3 ratio of ethanolic lipid mixture to aqueous buffer is generally used.). Continue vortexing the resulting dispersion for another 20–30 seconds. 1.2. Incubate the resulting solution at room temperature for up to 15 minutes. 1.3. After mixing, the LNPs were dialyzed against PBS (pH 7.4) for 2 h, sterile filtered using 0.2 μm filters, and stored at 4°C. 3. Microfluidic Mixing Method: 1.1 The 3 mL of siRNA buffer solution and 1 mL of the lipid mixture solution were mixed at a total flow rate of 12 ?mL/min (A 1:3 ratio of ethanolic lipid mixture to aqueous buffer is generally used.) in a microfluidic device.Note 5: Parameters such as the flow rate ratio and total flow rate can be altered to fine-tune LNPs. 1.2. After mixing, the LNPs were dialyzed against PBS (pH 7.4) for 2 h, sterile filtered using 0.2 μm filters, and stored at 4°C. Reference1. Curr Issues Mol Biol. 2022 Oct 19;44(10):5013-5027. 2. Curr Protoc. 2023;3(9):e898.
D-Lin-MC3-DMA, an ionizable cationic lipid, is a potent siRNA delivery vehicle.
体内研究：
含有二硬脂酰磷脂酰胆碱 (DSPC) 的脂质纳米颗粒 (LNP) 和可电离的氨基脂质，例如二亚油基甲基-4-二甲基氨基丁酸酯 (DLin-MC3-DMA) 是有效的体内 siRNA 运载工具。LNP-siRNA 系统经过优化以在小鼠静脉注射后的肝细胞中实现最大基因沉默效力，其中包含摩尔比为 50/10/38.5/1.5 的 DLin-MC3-DMA (MC3)、DSPC、胆固醇和聚乙二醇 (PEG)-脂质。DLin-MC3-DMA 具有优化的 pKa 值，可显著增强效力。
体外研究：
Preparation of MC3 Lipid NanoparticlesHere we provide lipid molar ratios for LNPs in FDA-approved Patisiran (a siRNA targets the transthyretin (TTR) mRNA). The molar ratio of lipids in this formulation is D-Lin-MC3-DMA : DSPC : Cholesterol : PEG2000-C-DMG = 50 : 10 : 38.5 : 1.5, and RNA to lipid weight ratio is 0.05 (wt/wt). A. Lipid Mixture Preparation1. Dissolve lipids in ethanol and prepare 10 mg/m stock solutions. The lipid stock solutions can be stored at ?20°C for later use.Note 1:The ionizable lipid is usually a liquid. Due to the viscosity, it should always be weighed rather than relying on the autopipette volume. Note 2: Cholesterol in solution should be kept warm (>37℃) to maintain fluidity. Transfer the cholesterol solution promptly to avoid cooling. 2. Prepare the lipid mixture solution as described. For each mL of lipid mixture add the following: 548 μL of 10mg/mL D-Lin-MC3-DMA (HY-112251), 254 μL of 10mg/mL Cholesterol (HY-N0322), 134 μL of 10mg/mL DSPC (HY-W040193), and 64 μL of PEG2000-C-DMG (HY-145411) . Mix the solutions thoroμghly to achieve a clear solution. This mixture contains 10 mg of total lipid. Note 3: The choice of lipids and ratios may be changed as desired and this will affect the LNP properties (size, polydispersity, and efficacy) and the amount of mRNA required. B. siRNA Preparation1. Prepare a 166.7 μg/mL siRNA solution with 100 mM pH 5 sodium acetate buffer. Note 4: The lipid:siRNA weight ratio influences the encapsulation efficiency. Other weight ratios may be prepared as alternative formulations and should be adjusted accordingly by user.C. MixingThere are three commonly used methods to achieve rapid mixing of the solutions: the pipette mixing method, the vortex mixing method, and the microfluidic mixing method. All these mixing methods can be used for various applications. It is important to note that pipette mixing method and vortex mixing method may yield more heterogeneous LNPs with lower encapsulation efficiencies and is prone to variability. Microfluidic devices enable rapid mixing in a highly controllable, reproducible manner that achieves homogeneous LNPs and high encapsulation efficiency. Within these devices, the ethanolic lipid mixture and aqueous solution are rapidly combined in individual streams. LNPs are formed as the two streams mix and are then collected into a single collection tube. 1. Pipette Mixing Method: 1.1. Pipette 3 mL of the siRNA solution and quickly add it into 1 mL of the lipid mixture solution (A 1:3 ratio of ethanolic lipid mixture to aqueous buffer is generally used.) Pipette up and down rapidly for 20–30 seconds. 1.2. Incubate the resulting solution at room temperature for up to 15 minutes. 1.3. After mixing, the LNPs were dialyzed against PBS (pH 7.4) for 2 h, sterile filtered using 0.2 μm filters, and stored at 4°C. 2. Vortex Mixing Method: 1.1. Vortex 3 mL of siRNA solution at a moderate speed on the vortex mixer. Then, Quickly add 1 mL of the lipid mixture solution into the vortexing solution (A 1:3 ratio of ethanolic lipid mixture to aqueous buffer is generally used.). Continue vortexing the resulting dispersion for another 20–30 seconds. 1.2. Incubate the resulting solution at room temperature for up to 15 minutes. 1.3. After mixing, the LNPs were dialyzed against PBS (pH 7.4) for 2 h, sterile filtered using 0.2 μm filters, and stored at 4°C. 3. Microfluidic Mixing Method: 1.1 The 3 mL of siRNA buffer solution and 1 mL of the lipid mixture solution were mixed at a total flow rate of 12 ?mL/min (A 1:3 ratio of ethanolic lipid mixture to aqueous buffer is generally used.) in a microfluidic device.Note 5: Parameters such as the flow rate ratio and total flow rate can be altered to fine-tune LNPs. 1.2. After mixing, the LNPs were dialyzed against PBS (pH 7.4) for 2 h, sterile filtered using 0.2 μm filters, and stored at 4°C. Reference1. Curr Issues Mol Biol. 2022 Oct 19;44(10):5013-5027. 2. Curr Protoc. 2023;3(9):e898.
产品资料
Copyright©2015-2024 沪ICP备2022026524号-1
沪公网安备