Vitamin-Mediated Cell Delivery of Oligonucleotides an Attractive Approach for Therapeutic Applications
Link Technologies Ltd, a specialist oligonucleotide reagent manufacturer, has announced the availability of a novel vitamin modifier, which has shown in initial tests to have the potential of improving cell delivery of oligonucleotides.
The new reagent, 5’-Niacin-CE Phosphoramidite, is easily incorporated during solid phase oligo synthesis. The niacin-based modifier from Link offers several advantages compared with the use of conventional lipophilic delivery agents, including reduced risk of in vivo toxicity, and removes the necessity of cleaving the delivery reagent once in the cell. These benefits make vitamins, including niacin, an attractive method for the delivery of therapeutic oligonucleotides, such as siRNA, into cells.
Although lipophilic modifier reagents have been shown to enhance cell penetration, vitamin-mediated cell delivery offers a distinct advantage due to the fact that vitamins are required, but not produced by cells. As such, it is believed that interaction with a specific binding protein is required before the vitamin-oligo conjugate is internalised. Not only does this enhance delivery and overcome the risk of toxicity, as the vitamin-based reagents are recognised by the cell, but it also offers some exciting potential for cell targeting.
Derived from niacin, an essential vitamin heavily involved in the biosynthesis of NAD and NADH, Link’s new vitamin modifier, 5’-Niacin-CE Phosphoramidite, is significantly less hydrophobic and less bulky than existing delivery agents. Whereas large lipophilic modifiers can supress an oligo’s function in vivo and therefore require cleaving, which is difficult to control, it is expected that with vitamin-based modifiers, intracellular cleavage of modifiers is not necessary. Potentially, this will lead to a reduction in required dosage of the therapeutic oligonucleotide, importantly minimising the risk of drug toxicity and side effects to the patient.
Catherine McKeen, Head of Technology Commercialisation, explained: “The ability to incorporate vitamin modifiers during oligo synthesis opens up significant potential to utilise a range of vitamin-oligonucleotide conjugates as a means of enhanced cellular uptake of therapeutic oligonucleotides. 5’-Niacin-CE Phosphoramidite is the second vitamin-based reagent in Link’s portfolio, alongside our tocopherol modifiers, and we will continue to add to this range.”
As an ISO 9001:2008 certified company, Link provides the novel modifier reagent in quantities ranging from milligramme to multi-gramme bulk scale, to support entire project life-cycles. Although protected by patent, Link is making this product available for purchase with an implied licence for research-use-only (RUO) applications, ensuring that the high potential of vitamin-mediated cell delivery can be easily accessed and validated in laboratories worldwide. To promote the uptake of the technology in commercial applications, Link welcomes approaches for such licences, and is committed to negotiating attractive terms to prospective commercial partners.
Related News
-
News US BIOSECURE Act passed by US House of Representatives
The controversial act, which has already impacted several foreign companies operating in the US, was passed by the House of Representatives on September 9, 2024. It is now headed for the US Senate before it can be signed into law by President Joe Biden... -
News Pharma Supply Chain People Moves
The latest appointments, promotions, and structural changes across the pharmaceutical supply chain. -
News Drug prices agreed upon as part of the US Inflation Reduction Act
The Inflation Reduction Act brought into constitution by the Biden administation in 2022, which proposed a drug price negotiation between the government and pharmaceutical companies, has reached it's first agreement. -
News BIOSECURE Act continues to loom over Chinese pharma manufacturers
With the US BIOSECURE Act on its way to passing into legislation, Chinese companies are facing declining revenues within the first half of 2024 as US pharmaceutical and healthcare companies pull their businesses from the country. -
News Ophthalmologic drug product Eylea faces biosimilar threats after FDA approvals
Regeneron Pharmaceutical’s blockbuster ophthalmology drug Eylea is facing biosimilar competition as the US FDA approves Biocon’s Yesafili and Samsung Bioepis/Biogen’s Opuviz. -
News ONO Pharmaceutical expands oncology portfolio with acquisition of Deciphera
ONO Pharmaceutical, out of Japan, is in the process of acquiring cancer-therapy maker Deciphera Pharmaceuticals for US$2.4 billion. -
News First offers for pharma from Medicare drug price negotiations
Ten high-cost drugs from various pharma manufacturers are in pricing negotiations in a first-ever for the US Medicare program. President Biden’s administration stated they have responded to the first round of offers. -
News Eli Lilly’s Zepbound makes leaps and bounds in weight-loss drug market
In the last week, Eli Lilly has announced their partnership with Amazon.com’s pharmacy unit to deliver prescriptions of Zepbound. Zepbound has also surpassed Novo Nordisk’s Wegovy for the number of prescriptions for the week of March 8.&nbs...
Position your company at the heart of the global Pharma industry with a CPHI Online membership
-
Your products and solutions visible to thousands of visitors within the largest Pharma marketplace
-
Generate high-quality, engaged leads for your business, all year round
-
Promote your business as the industry’s thought-leader by hosting your reports, brochures and videos within your profile
-
Your company’s profile boosted at all participating CPHI events
-
An easy-to-use platform with a detailed dashboard showing your leads and performance