Related Experiment Video
Updated: Jun 23, 2026

09:34
Extraction and Characterization of Surfactants from Atmospheric Aerosols
Published on: April 21, 2017
Synthetic surfactants: where are we? Evidence from randomized, controlled clinical trials
1Department of Neonatology, New Hanover Regional Medical Center, Wilmington, NC 28402-9025, USA. Fernando.moya@seahec.net
Summary
New synthetic surfactants with SP-B mimicry offer faster action and reduced respiratory distress syndrome (RDS) incidence, comparable to animal-derived options. These advancements improve short-term outcomes and long-term survival in infants.
Area of Science:
- Neonatal Medicine
- Pulmonary Medicine
- Biochemistry
Background:
- Exogenous surfactants are crucial for managing respiratory distress syndrome (RDS).
- Animal-derived surfactants containing surfactant proteins (SP)-B and SP-C show clinical advantages over synthetic colfosceril.
- Previous comparisons did not demonstrate improved overall mortality or bronchopulmonary dysplasia (BPD) with animal-derived surfactants.
Purpose of the Study:
- To evaluate the efficacy of a novel synthetic surfactant mimicking SP-B.
- To compare its clinical outcomes against colfosceril and animal-derived surfactants.
Main Methods:
- Head-to-head trials comparing different surfactant preparations.
- Analysis of short-term clinical outcomes and survival rates up to one year of age.
Main Results:
- Animal-derived surfactants demonstrated faster onset of action and reduced RDS incidence when used prophylactically.
- No significant differences in overall mortality or BPD were observed between animal-derived and colfosceril surfactants.
- The new synthetic surfactant improved short-term outcomes compared to colfosceril and showed comparable or superior survival to animal-derived surfactants at one year.
Conclusions:
- New-generation synthetic surfactants mimicking SP-B offer promising alternatives for RDS management.
- These agents provide clinical benefits including faster action and improved survival.
- Further research may solidify their role in neonatal respiratory care.
Related Concept Videos
Clinical Trials
Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
There are four phases in a clinical trial. A phase one...
Clinical Trials: Overview
Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
Surface Active Agents
Surfactants, named for their behavior at interfaces, positively adsorb at the interfaces of two phases, reducing interfacial tension. Their versatility as emulsifiers, detergents, and foaming agents stems from this ability. Surfactants, often termed amphiphiles, share the property of amphipathy, with molecules having both hydrophilic and hydrophobic portions. The hydrophilic part is called the head, and the hydrophobic part, including an elongated alkyl substituent, forms the tail.Surfactants...
Micelles
Micelle formation is an intricate process that hinges on the properties of amphiphilic or amphipathic molecules and the conditions of the system in which they are found. Amphiphilic molecules, which have both hydrophilic (water-attracting) and hydrophobic (water-repelling) parts, play a critical role in this process.In aqueous environments, these molecules arrange themselves such that their hydrophilic heads are turned towards the water phase, while their hydrophobic tails are oriented away...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Preclinical Development: Overview
Preclinical development consists of a series of tests that ensure the safety and efficacy of a new therapeutic compound before it is tested in humans. There are four main phases to this process. First, safety pharmacology tests are conducted to ensure the drug does not produce any acutely harmful effects. These tests examine parameters such as bronchoconstriction, cardiac dysrhythmias, blood pressure changes, and ataxia. Next, preliminary toxicological testing is performed to determine the...

