P2X7 receptor [5]

Eperisone对成纤维细胞活性的优先抑制作用[1]
我们筛选了临床常用药物库，旨在发现对肺泡上皮细胞无毒但对肺成纤维细胞具有选择性毒性的药物。具体而言，用不同药物处理LL29或A549细胞24小时后，采用甲基噻唑基四唑试剂检测细胞存活率。在LL29细胞IC50值低于A549细胞的药物中，基于两种细胞类型的IC50差异、临床安全性及其他药理活性，我们筛选出艾地苯醌和Eperisone。如前期报道，我们已证实艾地苯醌能优先抑制成纤维细胞活性并缓解博来霉素诱导的肺纤维化。因此本研究聚焦临床用作中枢性肌松剂的Eperisone，通过体外和体内系统评估其对特发性肺纤维化(IPF)的疗效。
如图1A所示，Eperisone处理(25-200μM)可剂量依赖性降低LL29细胞存活率。而200μM Eperisone处理的A549细胞存活率仍达88.5±3.0%(均值±标准误，n=4)，表明几乎不影响上皮细胞活性。此外，Eperisone对其他成纤维细胞(HFL-1和IMR-90)同样呈现剂量依赖性增殖抑制(补充图S1A)。在RL-34细胞(大鼠肝源正常上皮细胞)中几乎无毒性，但对可分化为肌成纤维细胞的RI-T细胞(大鼠肝星状细胞)具有优先抑制作用(补充图S1B)。我们进一步采用可检测细胞膜损伤的CellTox™绿色染料分析Eperisone对LL29的细胞毒性。如图1B所示，Eperisone处理呈现时间和浓度依赖性的细胞毒效应。为评估Eperisone对TGF-β1诱导的成纤维细胞活化影响，我们先用Eperisone(10-30μM)预处理LL29细胞，再添加TGF-β1(5μM)，72小时后通过实时定量PCR分析纤维化相关因子表达。如图1C所示，TGF-β1可上调LL29细胞中I型胶原(COL1A1)、α-SMA(ACTA2)、结缔组织生长因子(CTGF)、血管内皮生长因子(VEGF)、碱性成纤维细胞生长因子(bFGF)和血小板衍生生长因子(PDGF-A)的mRNA表达，而这些上调均被Eperisone预处理所抑制。这些结果提示Eperisone在体外能优先抑制肺成纤维细胞活性。

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其他药物对肺成纤维细胞存活率的影响[1]
如前言所述，吡非尼酮和尼达尼布是目前临床用于治疗IPF的抗纤维化药物。为明确Eperisone对肺成纤维细胞的特异性作用，我们比较了现有药物对LL29和A549细胞存活率的影响。吡非尼酮处理(浓度高达2mM)对两种细胞存活率均无显著影响；尼达尼布虽能降低两种细胞存活率，但抑制程度无细胞类型差异性(图2A)。
Eperisone作为中枢性肌松剂，临床用于改善腰痛和脑血管疾病所致痉挛性瘫痪患者的肌张力。因此我们检测了其他中枢性肌松剂是否具有成纤维细胞选择性。在六种测试药物中，甲苯哌丙酮、伊那哌酮和兰哌酮与Eperisone相似，可优先降低LL29细胞活力；而替扎尼定、美索巴莫和巴氯芬在浓度高达2mM时对两种细胞均无抑制作用(图2B)。如后文将讨论的，由于部分中枢性肌松剂未显示成纤维细胞选择性抑制，我们推测Eperisone可能通过独立于肌松作用之外的分子机制发挥其选择性效应。

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盐酸依哌立松于1983年在日本上市，已被用于改善肌肉张力和治疗痉挛性瘫痪。然而，其生化作用机制尚不清楚。SB药物发现用于使用荧光评估嘌呤能P2X（P2X）受体拮抗作用。在这项研究中，我们发现其靶蛋白是P2X7受体。此外，P2X受体亚型选择性很高。这一发现证明了（Eperison-P2X7-pain连锁）、P2X7作为药物靶点的有效性以及盐酸Eperisone药物重新定位的可能性[5]。

Eperisone对博来霉素(BLM)诱导肺纤维化的影响[1]
通过气管内给予BLM诱导雄性ICR小鼠肺纤维化模型。具体而言，在BLM给药10天后，根据体重变化率（排除溶剂对照组）将小鼠分为三组，考察口服Eperisone对肺纤维化的影响。BLM给药20天后制备肺组织切片，采用Masson三色染色法检测胶原沉积。结果显示肺组织胶原沉积呈现BLM剂量依赖性增加，而口服Eperisone则能剂量依赖性抑制这种BLM诱导的胶原沉积（图3A，B）。
随后我们对肺组织中胶原特异性氨基酸——羟脯氨酸进行定量分析。如图3C所示，BLM处理显著增加肺组织羟脯氨酸含量，而Eperisone处理可抑制这一增加。考虑到Eperisone治疗肺纤维化的临床应用价值，除组织学和生化指标外，改善呼吸功能同样至关重要。我们前期研究已证实BLM诱导的肺纤维化会导致肺弹性增加和用力肺活量(FVC)下降。因此本研究采用计算机控制呼吸机和负压储气装置检测小鼠呼吸功能。如图3D所示，BLM处理使总弹性（包括支气管、细支气管和肺泡的整个肺部弹性）和组织弹性（肺泡弹性）显著增加，并降低FVC；而Eperisone能显著改善BLM引起的呼吸功能恶化。这些结果表明Eperisone对BLM诱导的肺纤维化具有改善作用。

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目的：Eperisone是一种口服肌肉松弛剂，用于治疗引起肌肉痉挛和疼痛的肌肉骨骼疾病。为了更有效地控制疼痛，依匹立松通常与非甾体抗炎药（NSAIDs）一起服用。因此，与非甾体抗炎药相比，乙哌立松可能被忽视为过敏反应的原因。本研究旨在分析韩国报告的药物不良反应（ADR），并为乙哌立松引起的过敏反应提出适当的诊断方法。 方法：我们回顾了2010年至2015年韩国报告的与Eperisone相关的电子药物警戒数据（韩国药品安全研究所韩国不良事件报告系统[KIDS-KAERS]）。选择具有因果关系的ADR。分析了临床表现、严重程度、结果和再暴露信息。为了进一步调查，还审查了单个中心报告的7年ADR数据。该中心进行了口服激发试验（OPT）、皮肤点刺试验（SPT）和嗜碱性粒细胞活化试验（BAT）。 结果：在研究期间，207名患者对依哌立松有不良反应。最常见的不良反应是皮肤过敏反应（30.4%），如荨麻疹、瘙痒或血管性水肿。第五种常见的不良反应是过敏反应。有35名患者发生过敏反应，占依哌立松相关不良反应的16.9%。在单中心研究中，有11名患者发生了依哌立松引起的过敏反应。所有患者均接受了OPT，所有诱发患者均显示阳性反应。11名过敏反应患者中有4名也接受了SPT和BAT检查，结果均为阴性。 结论：根据KIDS-KAERS数据库计算的Eperisone诱导的过敏反应发生率为0.001%。依哌立松可引起超敏反应，包括过敏反应，可能是通过诱导非免疫球蛋白介导的立即超敏反应。

P2X Panel 筛选方案：将稳定表达P2X受体的细胞（P2X1受体为132N1星形细胞瘤细胞，其他P2X受体为HEK293细胞）以每孔50000个细胞的密度接种在黑色透明底96孔板中，并在37°C下孵育过夜。第二天，从细胞板中取出培养基，加入25µL的测定缓冲液（1.11 mM CaCl2、0.43 mM MgCl.6H2O、0.36 mM MgSO4.7H2O、4.98 mM KCl、0.39 mM KH2PO4、122 mM NaCl、0.3 mM Na2HPO4、4.86 mM D-葡萄糖、17.7 mM N-（2-羟乙基）哌嗪-N′-2-乙磺酸（HEPES），pH 7.4）。将钙染料溶液（10µL）加入孔中，在37°C下孵育1小时。加入试验化合物（5µL），在室温下孵育10分钟。然后将平板置于FLIPR中，每1.52秒监测一次荧光。20秒后，加入10µL约EC80浓度的激动剂，在488 nm/510-570 nm的ex/em下监测荧光5分钟。使用GraphPad Prism软件测定测试化合物的IC50值。YO-PRO-1摄取测定方案：将THP-1细胞以每皿10000000个细胞的密度接种到100mm培养皿上，用500 nmol/L佛波醇12-肉豆蔻酸13-乙酸酯处理3小时。收集细胞，用磷酸缓冲盐水（PBS）离心洗涤，并将细胞重新悬浮在培养基（10%胎牛血清（FBS）/RPMI1640）中。将细胞以80000个细胞/0.2 mL/孔的密度接种在黑壁96孔板中，并在37°C下孵育过夜。然后，在孔中加入脂多糖（LPS）（1µg/mL），并将细胞处理6小时（预处理）。用测试化合物处理细胞，将Yo-PRO-1（2µmol/L）加入孔中，在37°C下孵育15分钟。最后，在孔中加入BzATP（300微摩尔/升，P2X7受体激动剂），在ex/em:485nm/535nm下每1分钟监测一次荧光，持续60分钟。测量了10分钟的最大荧光斜率[5]。

Treatment of mice with BLM, Eperisone, and other reagents [1]
Mice were anesthetized with isoflurane and intratracheally administered BLM (1 mg/kg, once) in sterile saline via a single channel pipette (P200). Ten days after BLM administration, Eperisone (15 or 50 mg/kg), tolperisone (15 mg/kg), pirfenidone (200 mg/kg), and nintedanib (30 mg/kg) were administered orally for a total of 9 days from day 10 to day 18. Various analyses were then performed on day 20.
In the adverse effect study, 10 days after BLM administration, 250 mg/kg of Eperisone was orally administered once, which was five times the dose that showed efficacy. Twenty-four hours after eperisone administration, the fecal condition of the mice was visually examined. In addition, plasma samples and stomach and colon tissues were collected from the mice.

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Mice were treated with bleomycin (BLM, 1 mg/kg) or vehicle once only on day 0. The mice were then orally administered 250 mg/kg of eperisone (Epe) once at day 10. After 24 h, whole blood was collected from the mice. Analysis of the blood samples was performed by TRANS GENIC INC. Values represent the mean ± SEM.[1]

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Mice were treated with bleomycin (BLM, 1 mg/kg) or vehicle once only on day 0. The mice were then orally administered 250 mg/kg of eperisone (Epe) once at day 10. After 24 h, the fecal condition (diarrhea or hemorrhagic stool) of the mice was visually examined. The analysis of fecal condition was conducted by an investigator blinded to the study protocol. Gastric mucosal injury and colonic mucosal injury were analyzed based on the hematotoxin and eosin staining images shown in Fig. 5.[1]

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Mice were treated with bleomycin (BLM, 1 mg/kg) or vehicle once only on day 0. The mice were then orally administered 250 mg/kg of eperisone (Epe) once at day 10. After 24 h, the stomach and colon were collected from the mice. Gastric (A) and colonic (B) tissue sections were prepared and subjected to histopathological examination (hematotoxin and eosin staining; scale bar = 200 µm).[1]

123698trattLD50 toralt 1002 mg/kgt Sensory organs and special senses: Lacrimal: eyes; Autonomic nervous system: smooth muscle relaxant (mechanism unclear, antispasmodic); Behavior: seizures or effects on the epileptic threshold tYakuri to Chiryo. Pharmacology and Therapeutics., 19(1743), 1991
123698trattLD50 tsubcutaneoust 490 mg/kgt Behavior: excitation; Behavior: ataxia; Lung, pleural cavity or respiration: respiratory depression tOyo Yakuri. Pharmacology and Therapeutics., 21(939), 1981
123698trattLD50 tintravenoust 51 mg/kgt Behavior: excitation; Behavior: ataxia; Lung, pleural cavity or respiration: respiratory depression tOyo Yakuri. Pharmacology and Therapeutics., 21(939), 1981
123698trattLD50 tintravenoust 51 mg/kgt Behavior: excitation; Behavior: ataxia; Lung, pleural cavity or respiration: respiratory depression tOyo Yakuri. Pharmacology and Metrology, 21(939), 1981
123698trattLD50tintramusculart400 mg/kgtbehavior: excitation;behavior: ataxia;lung, pleural or respiratory: respiratory depressiontOyo Yakuri. Pharmacology and Metrology, 21(939), 1981
123698tmousetLD50toralt324 mg/kgttPharmacy Journal, 107(705), 1987 [PMID:3437397]

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Safety Analysis of Ipilizumab Dosage[1]
In clinical practice, existing drugs for the treatment of idiopathic pulmonary fibrosis (IPF), such as pirfenidone and nintedanib, have been reported to cause adverse reactions, such as elevated plasma markers of liver injury and gastrointestinal disorders. Therefore, we conducted a comprehensive analysis of plasma markers of pancreatic, liver and kidney injury. The dose of ipilisone was five times the effective dose for bleomycin-dependent pulmonary fibrosis. As shown in Table 1, neither bleomycin alone (BLM) nor bleomycin combined with ipilisone (250 mg/kg, single dose on day 10) significantly altered 12 plasma markers of pancreatic, hepatic, and renal injury. Furthermore, continuous administration of ipilisone (50 mg/kg) for 9 days (days 10 to 18) did not cause significant changes in four plasma markers of hepatic and renal injury (Supplementary Table S1). Additionally, no diarrhea or bloody stools were observed in either group of mice (Table 2). Furthermore, we used hematoxylin-eosin staining to detect gastric and colonic mucosal damage. As shown in Figure 5 and Table 2, compared with the vector control group, the gastric and colonic mucosal conditions of the bleomycin (BLM) group or the BLM combined with ipilisone (250 mg/kg) group were unchanged, and no gastric or colonic mucosal damage was observed. These results suggest that ipilisone may inhibit pulmonary fibrosis without causing adverse reactions.

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Ipilisone hydrochloride (4'-ethyl-2-methyl-3-piperidinylphenylacetone hydrochloride) is an antispasmodic drug used to treat conditions characterized by muscle stiffness and pain. This study aimed to investigate the efficacy of ipilisone in treating patients with acute low back pain and spinal muscle spasms. This randomized, double-blind (double-dummy) study included 160 patients with low back pain and no prior history of spinal disease. Patients were randomly assigned to receive oral ipilisone 100 mg three times daily (tid) or colchicine 8 mg twice daily (bid) for 12 consecutive days. Analgesic effects were assessed using the visual analog scale (VAS) for spontaneous pain and a four-point pain scale for activity/touch pain; muscle relaxation effects were assessed using hand-to-ground distance and the Lasseg test. All measurements were performed on the day of enrollment and on days 3, 7, and 12 of treatment. The analgesic and muscle relaxant effects of the two drugs were comparable. Both treatments significantly reduced spontaneous pain and pain on activity/touch. In addition, patients treated with both epirlisone and colchicine showed clinically significant muscle relaxation, manifested as a gradual reduction in the “hand-to-ground” distance and an increase in joint range of motion (Rasseger test). Only 5% of patients in the epirlisone group experienced mild gastrointestinal side effects, compared to 21.25% in the colchicine group. In addition, diarrhea was also observed in patients in the colchicine group, with some cases being moderate. In conclusion, epirlisone is an effective and safer alternative muscle relaxant for the treatment of low back pain. [2] Epirlisone is an analgesic central muscle relaxant that has been used to treat low back pain (LBP). This systematic review aimed to evaluate the efficacy and safety of epirlisone in the treatment of patients with low back pain. This systematic review followed the Cochrane Back and Neck (CBN) group and the Preferred Reporting Entries for Systematic Reviews and Meta-analyses (PRISMA) guidelines. Risk of bias was assessed using the CBN group and the Moga tool. A total of 7 studies were included (5 randomized controlled trials [RCTs] and 2 non-controlled studies), involving 801 participants. Epilisodesonide intervention may be effective for patients with acute low back pain with fewer adverse reactions (relative risk, 0.25; 95% confidence interval, 0.15-0.41; p<0.0001). Epilisodesonide can also improve paravertebral blood flow and has similar efficacy to tizanidine in patients with chronic low back pain. The sample size and follow-up time of the studies included in this review are small and insufficient to support the use of epilisodesonide for the treatment of low back pain. However, we recommend conducting well-designed, high-quality RCTs with larger sample sizes and longer follow-up times to confirm the clinical benefit of epilisodesonide in the treatment of acute or chronic low back pain. [3]

[1]. Therapeutic effects of eperisone on pulmonary fibrosis via preferential suppression of fibroblast activity. Cell Death Discov. 2022 Feb 8;8(1):52.
[2]. Efficacy and safety of eperisone in patients with low back pain: a double blind randomized study. Eur Rev Med Pharmacol Sci. 2008 Jul-Aug;12(4):229-35.
[3]. Clinical efficacy and safety of eperisone for low back pain: A systematic literature review. Pharmacol Rep. 2016 Oct;68(5):903-12.
[4]. Eperisone-Induced Anaphylaxis: Pharmacovigilance Data and Results of Allergy Testing. Allergy Asthma Immunol Res. 2019;11(2):231-240.
[5]. Eperisone Hydrochloride, a Muscle Relaxant, Is a Potent P2X7 Receptor Antagonist. Chem Pharm Bull (Tokyo). 2024;72(3):345-348.

1-(4-Ethylphenyl)-2-methyl-3-(piperidin-1-yl)propyl-1-one is an aromatic ketone, an N-propylpiperidine derivative in which the hydrogen at the propyl 2-position is replaced by a p-ethylbenzoyl group. It belongs to the piperidine class of compounds and is also an aromatic ketone.
Epipresonone is an antispasmodic drug that relaxes skeletal and vascular smooth muscle and exhibits various effects, such as reducing muscle rigidity, improving blood circulation, and inhibiting pain reflexes. This drug is not approved for use in the United States but is available in other countries such as India, South Korea, and Bangladesh.
See also: Daunorubicin (note moved to).

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Although the exact pathogenesis of idiopathic pulmonary fibrosis (IPF) is unclear, the transdifferentiation of fibroblasts to myofibroblasts triggered by alveolar epithelial cell damage and the production of extracellular matrix components such as collagen are important mechanisms in the development of IPF. In the lungs of IPF patients, the rate of fibroblast apoptosis is lower than that of alveolar epithelial cells, and this process is involved in the pathogenesis of IPF. We used a drug library containing approved drugs to screen for those that preferentially reduced the viability of LL29 cells (lung fibroblasts from IPF patients) rather than A549 cells (human alveolar epithelial cell line). After screening, we selected ipilisone, a clinically used centrally acting muscle relaxant. Ipilisone exhibits less cytotoxicity to A549 cells and preferentially reduces LL29 cell survival, while pirfenidone and nintedanib do not have this effect. Ipilisone also significantly inhibits the transforming growth factor-β1-dependent transdifferentiation of LL29 cells into myofibroblasts. In in vivo studies in ICR mice, ipilisone inhibited bleomycin (BLM)-induced pulmonary fibrosis, respiratory dysfunction, and fibroblast activation. In contrast, under the same experimental conditions, pirfenidone and nintedanib were less effective than ipilisone in inhibiting BLM-induced pulmonary fibrosis. Finally, we found that ipilisone did not cause adverse liver or gastrointestinal reactions in the BLM-induced pulmonary fibrosis model. Based on these results, we believe that ipilisone may be safer than existing therapies and provide greater therapeutic benefit to patients with idiopathic pulmonary fibrosis (IPF). [1]

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Although pirfenidone and nintedanib are currently used clinically to treat IPF, they are ineffective in some cases and have been reported to cause adverse reactions such as elevated liver injury markers, diarrhea, and dyspepsia. Therefore, in this study, we adopted a “drug repositioning strategy” to find safer and more effective treatments for IPF. The in vitro studies shown in Figures 1 and 2 showed that ipilisone (rather than pirfenidone or nintedanib) preferentially reduced the number of surviving fibroblasts. In addition, the in vivo studies shown in Figures 3 and Supplementary Figure S1 showed that ipilisone (rather than pirfenidone or nintedanib) inhibited the exacerbation of bleomycin (BLM)-induced pulmonary fibrosis. Furthermore, ipilisone did not cause adverse reactions such as elevated liver toxicity markers or gastrointestinal disorders. Therefore, we believe that ipilisone may be safer and more effective than pirfenidone or nintedanib, making it a better choice for treating idiopathic pulmonary fibrosis (IPF). After screening for drugs that selectively induce fibroblast death, we selected ipilisone and demonstrated its efficacy in an animal model of IPF induced by fibroblast activation. As mentioned above, there has never been a previous report demonstrating that ipilisone preferentially induces fibroblast death or effectively treats fibrosis models. However, fibrosis can also occur in other organs besides the lungs, such as the liver, heart, and kidneys. For example, in the liver, hepatic stellate cells are activated by stimulation such as TGF-β1 and transdifferentiate into myofibroblasts, which promote the production of extracellular matrix components such as collagen, thereby inducing liver fibrosis in diseases such as non-alcoholic steatohepatitis. In the kidneys, resident fibroblasts, pericytes, bone marrow-derived cells, and endothelial cells transdifferentiate into myofibroblasts and induce renal fibrosis. Therefore, activated myofibroblasts derived from fibroblasts also play a role in fibrosis in organs other than the lungs. Thus, ipilison can preferentially inhibit fibroblast activity, which may be effective not only in pulmonary fibrosis models but also in fibrosis models of other organs; therefore, the results of this study have broad application prospects for future research. [1]

C₁₇H₂₅NO

259.39

259.194

C, 78.72; H, 9.71; N, 5.40; O, 6.17

64840-90-0

Eperisone hydrochloride;56839-43-1

3236

Typically exists as solid at room temperature

0.994 g/cm3

386.8ºC at 760 mmHg

170-172ºC

137.4ºC

3.491

20.31

0

2

5

19

275

0

CCC1=CC=C(C=C1)C(=O)C(C)CN2CCCCC2

SQUNAWUMZGQQJD-UHFFFAOYSA-N

InChI=1S/C17H25NO/c1-3-15-7-9-16(10-8-15)17(19)14(2)13-18-11-5-4-6-12-18/h7-10,14H,3-6,11-13H2,1-2H3

1-(4-ethylphenyl)-2-methyl-3-piperidin-1-ylpropan-1-one

eperisone; 64840-90-0; Eperisone [INN]; Eperisona; (+-)-Eperisone; Eperisonum; Eperisonum [INN-Latin]; Eperisona [INN-Spanish];

2934.99.9001

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples

注意: 如下所列的是一些常用的体内动物实验溶解配方，主要用于溶解难溶或不溶于水的产品（水溶度<1 mg/mL）。 建议您先取少量样品进行尝试，如该配方可行，再根据实验需求增加样品量。

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注射用配方1: DMSO : Tween 80： Saline = 10 : 5 : 85 (如： 100 μL DMSO → 50 μL Tween 80 → 850 μL Saline)
*生理盐水/Saline的制备：将0.9g氯化钠/NaCl溶解在100 mL ddH ₂ O中，得到澄清溶液。
注射用配方 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (如： 100 μL DMSO → 400 μL PEG300 → 50 μL Tween 80 → 450 μL Saline)
注射用配方 3: DMSO : Corn oil = 10 : 90 (如： 100 μL DMSO → 900 μL Corn oil)
示例: 以注射用配方 3 (DMSO : Corn oil = 10 : 90) 为例说明, 如果要配制 1 mL 2.5 mg/mL的工作液, 您可以取 100 μL 25 mg/mL 澄清的 DMSO 储备液，加到 900 μL Corn oil/玉米油中, 混合均匀。

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注射用配方 4: DMSO : 20% SBE-β-CD in Saline = 10 : 90 [如：100 μL DMSO → 900 μL (20% SBE-β-CD in Saline)]
*20% SBE-β-CD in Saline的制备（4°C，储存1周）：将2g SBE-β-CD (磺丁基-β-环糊精) 溶解于10mL生理盐水中，得到澄清溶液。
注射用配方 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (如： 500 μL 2-Hydroxypropyl-β-cyclodextrin (羟丙基环胡精)→ 500 μL Saline)
注射用配方 6: DMSO : PEG300 : Castor oil : Saline = 5 : 10 : 20 : 65 (如： 50 μL DMSO → 100 μL PEG300 → 200 μL Castor oil → 650 μL Saline)
注射用配方 7: Ethanol : Cremophor : Saline = 10： 10 : 80 (如： 100 μL Ethanol → 100 μL Cremophor → 800 μL Saline)
注射用配方 8: 溶解于Cremophor/Ethanol (50 : 50), 然后用生理盐水稀释。
注射用配方 9: EtOH : Corn oil = 10 : 90 (如： 100 μL EtOH → 900 μL Corn oil)
注射用配方 10: EtOH : PEG300：Tween 80 : Saline = 10 : 40 : 5 : 45 (如： 100 μL EtOH → 400 μL PEG300 → 50 μL Tween 80 → 450 μL Saline)

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口服配方 1: 悬浮于0.5% CMC Na (羧甲基纤维素钠)
口服配方 2: 悬浮于0.5% Carboxymethyl cellulose (羧甲基纤维素)
示例: 以口服配方 1 (悬浮于 0.5% CMC Na)为例说明, 如果要配制 100 mL 2.5 mg/mL 的工作液, 您可以先取0.5g CMC Na并将其溶解于100mL ddH2O中，得到0.5%CMC-Na澄清溶液；然后将250 mg待测化合物加到100 mL前述 0.5%CMC Na溶液中，得到悬浮液。

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口服配方 3: 溶解于 PEG400 (聚乙二醇400)
口服配方 4: 悬浮于0.2% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 5: 溶解于0.25% Tween 80 and 0.5% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 6: 做成粉末与食物混合

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注意: 以上为较为常见方法，仅供参考， InvivoChem并未独立验证这些配方的准确性。具体溶剂的选择首先应参照文献已报道溶解方法、配方或剂型，对于某些尚未有文献报道溶解方法的化合物，需通过前期实验来确定（建议先取少量样品进行尝试），包括产品的溶解情况、梯度设置、动物的耐受性等。

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请根据您的实验动物和给药方式选择适当的溶解配方/方案：
1、请先配制澄清的储备液(如：用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液，按从左到右的顺序依次添加助溶剂，澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明，并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀/澄清；向上述体系中加入50 μL Tween-80，混合均匀/澄清；然后继续加入450 μL ddH2O (或 saline)定容至 1 mL；
3、溶剂前显示的百分比是指该溶剂在最终溶液/工作液中的体积所占比例;
4、 如产品在配制过程中出现沉淀/析出，可通过加热(≤50℃)或超声的方式助溶;
5、为保证最佳实验结果，工作液请现配现用！
6、如不确定怎么将母液配置成体内动物实验的工作液，请查看说明书或联系我们;
7、 以上所有助溶剂都可在 Invivochem.cn网站购买。