How does your body process medicine Cline Valry

Have you ever wondered what
happens to a painkiller, like ibuprofen,

after you swallow it?

Medicine that slides down
your throat can help treat a headache,

a sore back,

or a throbbing sprained ankle.

But how does it get where it needs
to go in the first place?

The answer is that it hitches
a ride in your circulatory blood stream,

cycling through your body in a race
to do its job

before it’s snared by organs
and molecules designed to neutralize

and expel foreign substances.

This process starts
in your digestive system.

Say you swallow an ibuprofen tablet
for a sore ankle.

Within minutes, the tablet starts
disintegrating in the acidic fluids

of your stomach.

The dissolved ibuprofen travels
into the small intestine

and then across the intestinal wall
into a network of blood vessels.

These blood vessels feed into a vein,

which carries the blood,
and anything in it, to the liver.

The next step is to make
it through the liver.

As the blood and the drug molecules
in it travel through liver blood vessels,

enzymes attempt to react with
the ibuprofen molecules

to neutralize them.

The damaged ibuprofen molecules,
called metabolites,

may no longer be effective as painkillers.

At this stage, most of the ibuprofen
makes it through the liver unscathed.

It continues its journey out of the liver,

through veins,

into the body’s circulatory system.

Half an hour after you swallow the pill,

some of the dose has already made it
into the circulatory blood stream.

This blood loop travels through every
limb and organ,

including the heart, brain, kidneys,
and back through the liver.

When ibuprofen molecules
encounter a location

where the body’s pain
response is in full swing,

they bind to specific target molecules
that are a part of that reaction.

Painkillers, like ibuprofen, block the
production of compounds

that help the body transmit pain signals.

As more drug molecules accumulate,

the pain-cancelling affect increases,

reaching a maximum within about
one or two hours.

Then the body starts efficiently
eliminating ibuprofen,

with the blood dose decreasing by half
every two hours on average.

When the ibuprofen molecules detach
from their targets,

the systemic blood stream carries
them away again.

Back in the liver, another small fraction
of the total amount of the drug

gets transformed into metabolites,

which are eventually filtered out
by the kidneys in the urine.

The loop from liver to body to kidneys
continues at a rate

of about one blood cycle per minute,

with a little more of the drug neutralized
and filtered out in each cycle.

These basic steps are the same for
any drug that you take orally,

but the speed of the process

and the amount of medicine that makes
it into your blood stream

varies based on drug,

person,

and how it gets into the body.

The dosing instructions
on medicine labels can help,

but they’re averages based on
a sample population

that doesn’t represent every consumer.

And getting the dose right is important.

If it’s too low,
the medicine won’t do its job.

If it’s too high, the drug
and its metabolites can be toxic.

That’s true of any drug.

One of the hardest groups of patients
to get the right dosage for are children.

That’s because how they process medicine
changes quickly, as do their bodies.

For instance, the level of liver enzymes
that neutralize medication

highly fluctuates
during infancy and childhood.

And that’s just one
of many complicating factors.

Genetics,

age,

diet,

disease,

and even pregnancy influence the body’s
efficiency of processing medicine.

Some day, routine DNA tests may be able
to dial in the precise dose of medicine

personalized to your liver efficiency
and other factors,

but in the meantime,

your best bet is reading the label

or consulting your doctor
or pharmacist,

and taking the recommended amounts
with the recommended timing.

你有没有想过在你吞下
布洛芬等止痛药后会发生

什么?

顺着喉咙滑下的药物可以帮助治疗头痛

、背部酸痛

或扭伤的脚踝。

但它首先是如何到达它需要
去的地方的呢?

答案是它
在你的循环血液中搭便车,

在你的身体中循环,

在它被
设计用来中

和和排出外来物质的器官和分子困住之前完成它的工作。

这个过程
从你的消化系统开始。

假设您
因脚踝疼痛而吞下布洛芬片。

几分钟内,药片开始
在胃的酸性液体

中分解。

溶解的布洛芬
进入小肠

,然后穿过肠壁
进入血管网络。

这些血管进入静脉

,将血液
及其中的任何东西输送到肝脏。

下一步
是通过肝脏。

当血液和其中的药物
分子通过肝血管时,

酶会试图与布洛芬分子发生反应

以中和它们。

受损的布洛芬分子(
称为代谢物)

可能不再作为止痛药有效。

在这个阶段,大部分
布洛芬都能毫发无损地通过肝脏。

它继续离开肝脏,

通过静脉

进入身体的循环系统。

在你吞下药丸半小时后,

一些剂量已经
进入循环血液。

这个血液循环流经每一个
肢体和器官,

包括心脏、大脑、肾脏,
然后返回肝脏。

当布洛芬分子
遇到

身体疼痛
反应如火如荼的位置时,

它们会与
作为该反应一部分的特定目标分子结合。

止痛药,如布洛芬,会阻止

有助于身体传递疼痛信号的化合物的产生。

随着更多药物分子的积累

,消除疼痛的效果会增加,

大约在
一两个小时内达到最大值。

然后身体开始有效地
消除布洛芬

,血液剂量
平均每两小时减少一半。

当布洛芬分子
与其目标分离时

,全身血流会将
它们再次带走。

回到肝脏,
药物总量的另一小部分

转化为代谢物

,最终
通过尿液中的肾脏过滤掉。

从肝脏到身体再到肾脏的

循环以每分钟大约一个血液循环的速度继续,在每个循环中都会

有更多的药物被中
和并被过滤掉。

这些基本步骤
对于您口服的任何药物都是相同的,

但过程的速度

和进入血液的药物量因药物、人

以及药物进入体内的方式而异。

药品标签上的剂量说明可能会有所帮助,

但它们是
基于样本人群的平均值

,并不代表每个消费者。

获得正确的剂量很重要。

如果它太低,药物将无法发挥作用。

如果它太高,药物
及其代谢物可能有毒。

任何药物都是如此。

最难
获得正确剂量的患者群体之一是儿童。

那是因为他们处理药物的方式
变化很快,他们的身体也是如此。

例如,中和药物的肝酶水平

在婴儿期和儿童期高度波动。

这只是
众多复杂因素之一。

遗传、

年龄、

饮食、

疾病,

甚至怀孕都会影响身体
处理药物的效率。

有朝一日,常规 DNA 测试可能会

根据您的肝脏效率
和其他因素调整精确的药物剂量,

但与此同时,

您最好的选择是阅读标签

或咨询您的医生
或药剂师,

并服用推荐量
与推荐的时间。