
Exosomes: the best skin and beauty secret to know
Many of us haven't heard of exosomes, although they have been used for a few years by clinics and doctors in skin treatments. But now that skincare brands have started to use them in their products, those of us dedicated to trying to improve our complexions will be finding out all about them.
Naturally occurring in our bodies, exosomes are microscopic vesicles — structures containing liquids, almost like tiny water balloons — that transport proteins and lipids between cells. What makes them particularly useful is that they also communicate with cells. Which means, according to Dr Jonathan Dunne, a consultant plastic surgeon and the founder of the aesthetic clinic Montrose London which uses plant-based exosomes, that 'they can stimulate production of substances such as collagen and elastin, which are critical for healthy and youthful skin'. Both of those deplete as we age. But when exosomes locate cells that are flagging, they boost them back into action.
Cell-regenerating products are nothing new — retinoids, for example, have long been lauded for their ability to help to boost the production of new skin cells. But exosomes, when applied topically, are even better, says Rebecca Cullen-Smith, the education director at the skincare brand Dermalogica. The company has recently launched its Exo Booster, containing exosomes made using bacteria. These, she says, are biocompatible with our skin, and as efficacious if not more so than bovine — or human — derived exosomes, the latter being popular in Asia but not legal for cosmetic use in the UK.
• This article contains affiliate links that can earn us revenue
The difference between what retinoids and exosomes do, Cullen-Smith says, is that 'retinoids can signal cells to switch biological processes on and off by bonding to specific receptor proteins that drive actions such as strengthening collagen production' whereas 'exosomes are much more complex structures. They not only signal to cells, but also provide critical biological components that are required for specific functions.' In other words, they can stimulate cells to perform actions such as produce collagen and increase elasticity. (According to a paper last year for the International Journal of Biological Sciences, they can also help to suppress inflammation, promote tissue repair and help tissue regeneration.)
What difference will they make when looking in the mirror? Other than seeing the brightening and lifting effects from the facial or microneedling treatment during which exosomes would typically be applied like a serum, not a lot — they won't immediately change the appearance of skin like dermal fillers would.
But they should improve things over time, as the skin's natural repairing processes are triggered and sped up, resulting in smoothed lines, improved texture and tone, and a plumper, fresher complexion. This, consultants say, usually happens within a month after the treatment. (One third-party clinical trial which compared microneedling alone and microneedling with exosomes showed that the latter produced an impressive 86 per cent greater reduction in wrinkle appearance after three weeks.) For long-lasting results, a course of three treatments is recommended.
Katharine Mackenzie Paterson, a London facialist who has started offering bacterial and plant-based exosome treatments to clients, says they can also calm inflammation and restore damaged skin 'so they're perfect for anyone with sensitive or sensitised skin'.
• In-clinic cosmetic treatments and at-home gadgets to get now
After trying exosome treatments for a few weeks, with Dermalogica and KMP, both of our testers attested to good skin, day after day. 'Like you've consistently had your eight hours of sleep,' said one, with both commenting on how little foundation they're having to wear after their first session. And isn't that, after all, just what we want? Not an altered face — but a refreshed one.
Exosome treatments cost from £330 at Dermalogica, dermalogica.co.uk; £595 at Katharine Mackenzie Paterson for microneedling exosome treatment, kmpskin.com; £495 at Montrose London, montroseclinics.com
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


The Guardian
28 minutes ago
- The Guardian
Esther Rantzen hails Commons passage of ‘rigorous and safe' assisted dying bill
The assisted dying bill, if it becomes law, would remove the burden of seeing a loved one die in pain, the campaigner Esther Rantzen has said, insisting its backers have got right the balance between giving help to those who ask for it and protecting vulnerable people. The terminally ill adults (end of life) bill cleared the Commons with a majority of 23 votes on Friday, but must yet be debated by the Lords before returning to the Commons for consideration of any amendments they may make. 'I think people misunderstand when somebody says 'one of the reasons I wanted assisted dying was I didn't want to be a burden'. Well, that's how I feel in the sense that, if I die in agony, that memory will be a burden for my family. Not because I'm awkward or inconvenient, I may be both those things, but because nobody wants to see a loved one die in pain. Nobody wants that,' Rantzen told BBC Radio 4's Today programme on Saturday. Asked if she had any doubts about the detail of the bill, she added: 'I think we have got this right. Having the committee stage [in parliament], with that committee rigorously looking at every clause and deciding to set up a multidisciplinary panel of social workers, someone versed in psychology, someone legal, so that they could examine it in each case.' She added this 'makes it so rigorous and so safe. And, in other countries around the world which we've looked at because they've had assisted dying legalised for some time, it has not produced coercion.' The legislation could face a difficult passage through the Lords, with critics poised to table amendments to add further restrictions and safeguards to the bill. And it was suggested to Rantzen that peers could also choose to debate it for so long that it simply runs out of parliamentary time. 'I don't need to teach the House of Lords how to do their job. They know it very well, and they know that laws are produced by the elected chamber. Their job is to scrutinise, to ask questions, but not to oppose.' Rantzen, who turns 85 on Sunday and has terminal cancer, acknowledged the legislation would probably not become law in time for her to use it and she would have to 'buzz off to Zurich' to use the Dignitas clinic. The Paralympian and crossbench peer Baroness Tanni Grey-Thompson told BBC Breakfast: 'We're getting ready for it to come to the Lords and, from my personal point of view, about amending it to make it stronger … I do think there are a lot more safeguards that could be put in.' And the Conservative peer and disability rights campaigner Lord Shinkwin said the narrow Commons majority underlined the need for peers to take a close look at the legislation. Labour MP Kim Leadbeater, who steered the bill through the Commons, said she hoped peers would not seek to derail the legislation, which could run out of parliamentary time if it is held up in the Lords. 'I would be upset to think that anybody was playing games with such an important and such an emotional issue.'


BBC News
34 minutes ago
- BBC News
'I was unable to walk, talk, or recognise myself after coma'
A man who awoke from a three-month coma with no memory of who he was, says helping others in the same position has given him "purpose". Jamil Hussain, 35, from Lockleaze in Bristol, suffered multiple seizures behind the wheel whilst driving down the M69 during the first Covid-19 lockdown in 2020. He was soon diagnosed with limbic encephalitis - a rare neurological condition that causes inflammation in the brain, leading to epilepsy and severe memory Hussain now acts as a mentor at Henbury's Cygnet Brunel health centre, where he spent 18 months relearning how to walk, talk, and live independently again. "When I woke up, I didn't know who I was or how to do anything," he said. "I couldn't walk, talk or even recognise most people - only my mum. I remember seeing her and knowing who she was but not being able to speak. It was terrifying."He said it was the "scariest" moment of his life and it was his mother who helped him through, despite medics originally telling his family his chance of recovery was "slim".The sight of her familiar face triggered a faint memory of "comfort and safety", which he says "brought him back to reality". He believes that moment forever changed the trajectory of his life."Whenever I feel angry or impulsive, I just remember that moment and think 'that's how close you were to not being able to know anything about yourself, ever again'."I could have been in the hospital for the rest of my life, waiting for my brain to put the pieces back together. I was so lucky, and that keeps me level-headed," he added. In his role as an Expert by Experience, Mr Hussain draws upon his own ordeal to comfort patients and "help them see a way through" their diagnoses."I want to be that beacon of light for others who are in still in the thick of their difficult times, helping them see a way through," he work also involves coaching staff and helping patients feel reassured by someone who's walked in their shoes."I want to show people there is light at the end of the tunnel. Life can be even better than it was before. It gives me purpose," he added.


BBC News
34 minutes ago
- BBC News
British couple win visa battle after MS deportation fear
A British couple who feared being deported from Australia after one of them was diagnosed with multiple sclerosis (MS) say they are "proud" to have been granted permanent Mathers, originally from Cheshire, had previously been told the potential cost of treating her condition for the health services meant a previous application alongside her boyfriend Rob O'Leary had been couple appealed against the decision in 2023 and launched an online petition earlier this year calling for Australia's minister for home affairs to review their recently shared they had been granted a visa after "a nearly four-year-long, emotional road". In their latest post, they said: "We are proud to announce we are Australia's newest Permanent Residents!"They added they were "over the moon" when their MP Allegra Spender told them that Tony Burke, minister for immigration, "personally contacted her to confirm the decision". Ms Mathers and Mr O'Leary, from London, met while backpacking in the country in 2017 and have lived there ever 2020, she was diagnosed with the relapsing-remitting variant of MS, which is a neurological condition with symptoms including muscle stiffness and difficulties in walking and Mathers received treatment in Australia under a reciprocal health agreement with the UK and said her condition had been "well managed" so the couple's requests for permanent residency were rejected in 2023 due to the costs linked to her medical entering Australia must meet certain health requirements, including not having "unduly increasing costs" for the country's publicly-funded healthcare service Medicare. Mr O'Leary said they had offered to pay the medical costs themselves or take out private insurance, adding that "the law is black and white, and the refusal is based on that, it's really hard for us".Their petition, which drew more than 25,000 signatures, called on Australia's minister for home affairs to review their case and look into immigration policies that "unfairly target individuals with well-managed health conditions". Mr O'Leary, who works in the construction trade, and his partner, who is a project manager and DJ, were "not asking for special treatment" but a chance to continue "working hard to contribute to this country in meaningful ways".In their latest post, they thanked supporters and said "there are so many things we've put on hold - just in case we had to leave"."But now, with this door wide open, we feel more focused and excited than ever to build our future in the country we love."Our families are overjoyed and already thinking of planning a trip to celebrate with us." See more Cheshire stories from the BBC and follow BBC North West on X.