
RoadRash said:the vast majority of the peptides sold by Lilly and Novo Nordisk are manufactured in China under contract by these companies.

Yes we are. Just a simple Google search will give you several companies in CN that manufacture for the two big GLP companies. Many of the CN companies were started with venture capital money from the US big pharma industries . It’s a fact.krsct said:Are we really sure that this is true? How do we know?


Jellybelly54 said:Yes we are. Just a simple Google search will give you several companies in CN that manufacture for the two big GLP companies. Many of the CN companies were started with venture capital money from the US big pharma industries . It’s a fact.

太棒了!恭喜!!ghreid said:我也是一名医生,当我的心脏病专家建议我考虑使用GLP-1时,我做了些研究。由于医保不涵盖,品牌药每月要花费我875美元。我的家庭医生建议我去配药药房,这样价格降到了每月285美元。在发现灰色市场并阅读了《新英格兰医学杂志》上关于零售药房的文章后,我决定尝试一下。我的医生们对我的效果非常满意(减重100磅),并且一直在密切关注我的进展。现在我开始深入研究其他肽类药物了。

现在还有合法的配药商吗?还是只是那些还没收到停止销售通知书的?是的,他们的原料来源都一样。以前(或者说现在)有一些美国公司声称自己会进行原料的冻干处理,但我不知道现在是否属实。这里有些人对这方面比较了解,或许有更确切的信息。krsct said:我猜想,美国合法的药品生产商也是从这些公司采购的吧?
他们没有说明货源。不过,大型制药公司曾表示他们不向配药商出售这些药物,所以它们肯定有来源。krsct said:我猜想,美国合法的药品生产商也是从这些公司采购的吧?

美国食品药品监督管理局 (FDA) 有一份全球范围内获得 FDA 批准的药品生产商名单,这些生产商生产的药品可以进口到美国,并由符合 503a 或 503b 条件的药房进行配制。像礼来公司这样的制药企业无需被归类为 503a 或 503b 药房,因为他们的最终产品已经过 FDA 的测试和批准。礼来公司在北卡罗来纳州从中国进口大量原料药,然后进行测试、加工和包装,最终制成注射笔,销往世界各地。neo6488 said:他们没有说明货源。不过,大型制药公司曾表示他们不向配药商出售这些药物,所以它们肯定有来源。

Jellybelly54 said:是的,我们是。只需简单地在谷歌上搜索一下,你就会发现中国有很多公司为两家大型GLP制药公司代工生产。许多中国公司最初都是由美国大型制药公司的风险投资启动的。这是事实。


RetCurious said:Jano 在他的实验室常见问题解答中提到,中国有 2 个原料肽的来源。

这是一份很棒的文件。RetCurious said:Jano 在他的实验室常见问题解答中提到,中国有 2 个原料肽的来源。

这篇采访报道写得不错,但需要注意的是,他提到Reta(一种较新的、结构更复杂的肽)可能有两个来源。他的解释也很有道理,关键在于成熟生产工艺的成本效益。而那些较老、稀有且结构相对简单的肽(例如GHK-Cu)可能拥有更多的生产商,Sema和Tirz也是如此。化学家可以联系中国多家不同的原料生产商(他们可能也提供冻干服务)来生产小批量(<100克)的肽。当然,价格肯定不会是0.2-0.5美元/毫克。RetCurious said:Jano 在他的实验室常见问题解答中提到,中国有 2 个原料肽的来源。

FilterOrDeath said:我总是很惊讶有些人竟然不这么做。![]()
Google Gemini said:At home, every time you move your arm to reach for a vial, you are shedding thousands of skin cells and bacteria (like Staph) into the air current.
Real cleanrooms use positive pressure to push air out. A home setup usually has neutral or negative pressure, meaning every time a door opens in the house, a "plume" of dust and pet dander is pulled toward the workspace.
A syringe filter catches bacteria, but it doesn't kill them. If your technique is slow, you are essentially concentrating contaminants onto a membrane and then high-pressuring your peptide solution through that "bio-mat."

After filtering my last couple vials I just have the feeling that with all the steps(multiple syringes, multiple pokes, new vials/carts) just increases my chances of introducing contamination. I'm betting someone real smart could do some cool probabilities. I'd be betting that would show it to be a wash unless you were taking some extreme steps(or have access) with a sterile working environment.Calm Logic said:To play devil's advocate: How many airlocks to get to your ISO 5 cleanroom?
Often the reluctance with filtering is the concern that one may be creating a bigger problem.


Not surprising that someone with practical lab experience is a proponentFilterOrDeath said:Yes I'm still surprised when people don't filter. So I ask and try and add some levity to the question because I am curious. And a lot of the new people don't know about it so never considered it as an option to implement or ignore.
I personally don't think the process is difficult at all but I have worked in a lab before. I don't use pens either but the ones that do have a lot of experience doing the entire process already so it's easy to just add the filter during that step for them. And I don't completely agree with the Gemini AI answer, they are almost always inaccurate in some way or put their best guess in there, it's wild. My own thought process has always been that we have zero control over what happened to it when it was created, the quality or cleanliness of the labs, or in shipping etc. It's the grey market so we just accept that. But I do have control over the filtering and the quality of sterilization of the products I buy. I know which process was used in the sterilization and the materials they are made of etc. Even if it only filters out bacteria, tiny pieces that didn't dissolve, or debris of some kind 1 time it is worth it for me. It's just my personal preference to do it every time and I'm curious why others do not and their thought process. I have had one person say it was the added cost. Another say they didn't know if they could keep the area clean to do it properly until they got the 70% alcohol spray. I see some here worry that it could cause the issue. And far more did not know what it is.
There are people on here that don't filter or even change needles every time and that's fine for them.We all decide what we are willing to try so it's good to have the information to make that decision.