A century of development history of peptide drugs
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A century of development history of peptide drugs: meet new challenges again
A century of development history of peptide drugs. Nearly a century since insulin entered clinical use, more than 80 peptide drugs have been approved for the treatment of various diseases, including diabetes, cancer, osteoporosis, multiple sclerosis, HIV infection and chronic pain.
With the advancement of technology, a hundred years after the discovery of peptide drugs, especially in the past 60 years, rapid development has been achieved, but the development of new drugs in this field is also facing new challenges.
From discovery to rapid development
Although the field of peptide therapy began with the first extraction of insulin from animal pancreas in 1922, with technological advancement, the scale of peptide production was expanded through liquid-phase chemical synthesis of peptides in the 1950s, and it was truly industrialized. An important step.
In determining the importance of peptides as new drugs, as well as their remarkable efficacy, selectivity and low toxicity, they also recognized their limitations, including low oral bioavailability, low plasma stability and short circulation time. In addition, liquid-phase chemical synthesis of peptides takes months to years, and the high cost of large-scale peptide production makes most pharmaceutical companies prohibitive. Therefore, only peptide hormone agonists that are effective at low doses are commercially viable. This has led to limited interest in peptides by the pharmaceutical industry and stalled the development of peptide drugs.
It was not until the invention of solid-phase peptide synthesis (SPPS) in 1963 and the development of purification technology that the field really entered the fast lane of development.
However, the use of peptides as subtype-selective probes for receptor research and continued development as lead compounds laid the foundation for the second wave of peptide drug development that began in the late 1980s. This time, the peptide drug development boom has been supported by venture funds and biotechnology companies. Human insulin produced using recombinant technology (approved in 1982) and the synthetic gonadotropin-releasing hormones leuprolide and goserelin (approved in 1985 and 1989, respectively) have been commercially successful, confirming the peptide The feasibility of the drug-like market and advances in drug delivery system technology, formulations and synthesis methods have promoted the rise of investment and research enthusiasm in this field. Therefore, the number of new peptide drugs that entered clinical trials from 2000 to 2010 was almost twice that in the 1990s.
It is worth mentioning that Exenatide has become the most successful class of GLP1 receptor agonists. It was approved for the treatment of type 2 diabetes in 2005, thus opening up new peptide drugs represented by GLP1 receptor agonists. era. Since then, several other GLP1 agonists have also been approved for the treatment of type 2 diabetes, including liraglutide, abiglutide, dulaglutide, lixisenatide and smeglutide, some of which have also been obtained Obesity indications are approved or other indications for metabolic diseases are being studied.
From the perspective of the global pharmaceutical market in 2019, peptide drugs accounted for 5% of the global pharmaceutical market, and the global sales of this category of drugs exceeded US$50 billion. In the past six decades, with the steady increase in peptide drug approvals, the average growth rate of the global peptide therapeutic drug market was 7.7%. Among them, insulin and its analogs accounted for about 50% of the peptide drug market (25 billion US dollars), followed by glucagon-like peptide 1 (GLP1) receptor agonists, dulaglutide Trulicity ( US$4.4 billion), liraglutide (Victoza and Saxenda) for the treatment of diabetes and obesity (US$4.1 billion), and the synthetic gonadotropin-releasing hormone analogue leuprolide (Lupron and Saxenda) for the treatment of cancer. Eligard) (US$2 billion).
At present, about 80 peptide drugs have been approved on the global market. The biopharmaceutical industry is steadily conducting research on new peptides and new drugs. There are more than 150 peptides in clinical development, and 400-600 peptides are undergoing clinical trials. Pre-research. With the increase in investment and research in the peptide field, peptide synthesis technology is becoming more mature, and it is expected that the peptide therapeutic drug market will continue to maintain its growth momentum.
Faced with new challenges again, great room for future development
Although great progress has been made in the field of peptide drugs, there is still much room for improvement and new development in overcoming key challenges.
01 Overcoming kidney clearance
Unmodified peptides are quickly cleared from the plasma (within a few minutes). Therefore, strategies to increase the molecular weight of peptides, such as lipidation, eulinky with larger proteins, and pegylation, will greatly increase its circulation in the blood. time.
Drugs that use lipid binding moieties in approved peptide drugs include C14/16/18 fatty acids linked to insulin detemir, insulin deglubber, liraglutide, and smeglutide to produce longer-acting analogs , Can be administered once a day or once a week (such as smeglutide).
Selective binding of serum albumin or immunoglobulin (two plasma proteins with unusually long circulation times, up to several weeks) is another strategy that extends the action time by exceeding the molecular weight cut-off of glomerular filtration. This strategy is used in drugs such as abiglutide and dulaglutide to extend the half-life, allowing one injection per week.
In addition, in the past two decades, the PEGylation of polyethylene glycol (PEG) chains attached to peptides or proteins has been developing rapidly. The FDA has approved a variety of PEGylated proteins (such as PEG-adenosine). Deaminase and PEG-α-interferon). In May 2019, Haosen Pharmaceutical’s innovative drug polyethylene glycol loxenatide injection (trade name: Fulaime) was approved to be marketed in some countries for the treatment of type 2 diabetes. It only needs to be injected once a week.
02 Drug delivery system seeks diversification
Most peptide drugs are administered by injection, so there are some disadvantages, including poor patient compliance, accidental injury, risk of infection, improper use, and waste of biohazard needles. Therefore, the development of alternatives based on needle injection has become a top priority.
Other methods of delivering drugs to the skin without injections include needle-free injection (jet injection). However, needle-free injections may cause pain and bleeding at the injection site, and there are differences in the amount of drug delivered, partly due to differences in skin characteristics between patients. Other methods include methods aimed at temporarily destroying the structure of the skin, such as the use of permeable polypeptides, and the use of ultrasound or electric fields to increase skin permeability. The microneedle technology used to deliver insulin or abaloparatide is in phase II and phase III trials, respectively.
Pulmonary route administration is another potential delivery route for peptides, but it has the problems of safety and limited delivery efficiency. Inhaled insulin (Pfizer’s Exubera) was approved by the FDA in 2006, but production was discontinued in 2007 due to safety considerations and high costs. With the development of the world’s second inhaled insulin product, MannKind’s Afrezza (approved by the FDA in 2014), we hope to reawaken people’s interest in the route of administration, but Afrezza still has potential safety hazards, and its side effects include cough or throat irritation .
Nasal delivery is another possible route of delivery of peptides, and desmopressin can be used as a nasal spray. However, as with the pulmonary route of administration, the impact of long-term delivery on sensitive mucosa is still worthy of attention. Therefore, these delivery routes may be more suitable for occasional use; for example, glucagon can be used as a dry nasal spray to treat severe hypoglycemia.
At present, the pharmaceutical industry has invested a lot of energy in developing strategies for the oral administration of peptide drugs, which is limited by the digestion of enzymes in the gastrointestinal tract and its limited penetration in intestinal epithelial cells. One of the strategies to overcome these obstacles is to co-formulate with penetration enhancers, which has achieved significant clinical success.
In 2019, the FDA approved the formulation of simaglutide and the penetration enhancer N-[8-(2-hydroxybenzoyl)amino]caprylate (SNAC) for oral administration once a day for the treatment of type 2 diabetes. SNAC is a small molecule fatty acid derivative, which can promote the absorption of smeglutide on the gastric mucosa by influencing the transcellular pathway. In June 2020, the FDA approved Chiasma’s oral administration of octreotide product Mycapssa using transient permeability enhancer (TPE) technology for the long-term treatment of acromegaly patients who are effective and tolerant to octreotide or lanreotide.
Maintenance therapy, this drug is the first and only oral somatostatin analogue (SSA) approved by the FDA. The oral insulin drug candidate (ORMD-0801) jointly developed by Hefei Tianmai Biology and Israel Oramed Company, including penetration enhancers, soybean trypsin inhibitors and chelating agents, is in phase III trials.
Although important progress has been made in the field of peptides, if major breakthroughs can be made in the fields of molecular biology and peptide chemistry, there is still a lot of room for development in the field of peptide therapy.
(source:internet, reference only)
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