News
Breastfeeding device measures babies’ milk intake in real time
While breastfeeding has many benefits for a mother and her baby, it has one major drawback: It’s incredibly difficult to know how much milk the baby is consuming.
To take the guesswork out of breastfeeding, an interdisciplinary team of engineers, neonatologists and pediatricians at Northwestern University has developed a new wearable device that can provide clinical-grade, continuous monitoring of breast milk consumption.
The unobtrusive device softly and comfortably wraps around the breast of a nursing mother during breastfeeding and wirelessly transmits data to a smartphone or tablet. The mother can then view a live graphical display of how much milk her baby has consumed in real time.
By eliminating uncertainty, the device can provide peace of mind for parents during their baby’s first days and weeks. In particular, the new technology could help reduce parental anxiety and improve clinical management of nutrition for vulnerable babies in the neonatal intensive care unit (NICU).
To ensure its accuracy and practicality, the device endured several stages of rigorous assessments, including theoretical modelling, benchtop experiments and testing on a cohort of new mothers in the hospital.
“Knowing exactly how much milk an infant is receiving during breastfeeding has long been a challenge for both parents and healthcare providers,” said Northwestern’s John Rogers, who led the device development.
“This technology eliminates that uncertainty, offering a convenient and reliable way to monitor milk intake in real time, whether in the hospital or at home.”
“Uncertainty around whether an infant is getting sufficient nutrition can cause stress for families, especially for breastfeeding mothers with preterm infants in the NICU,” said Dr. Daniel Robinson, a Northwestern Medicine neonatologist and co-corresponding author of the study.
“Currently, only cumbersome ways exist for measuring how much milk a baby has consumed during breastfeeding, such as weighing the baby before and after they have fed. We expect this sensor to be a big advance in lactation support, reducing stress for families and increasing certainty for clinicians as infants make progress with breastfeeding but still need nutritional support.
“Reducing uncertainty and helping families achieve their breastfeeding goals will lead to healthier children, healthier mothers and healthier communities.”
Diagnosis
Lung cancer drug shows breast cancer potential
Ovarian cancer cells quickly activate survival responses after PARP inhibitor treatment, and a lung cancer drug could help block this, research suggests.
PARP inhibitors are a common treatment for ovarian cancer, particularly in tumours with faulty DNA repair. They stop cancer cells fixing DNA damage, which leads to cell death, but many tumours later stop responding.
Researchers identified a way cancer cells may survive PARP inhibitor treatment from the outset, pointing to a potential way to block that response. A Mayo Clinic team found ovarian cancer cells rapidly switch on a pro-survival programme after exposure to PARP inhibitors. A key driver is FRA1, a transcription factor (a protein that turns genes on and off) that helps cancer cells adapt and avoid death.
The team then tested whether brigatinib, a drug approved for certain lung cancers, could block this response and boost the effect of PARP inhibitors. Brigatinib was chosen because it inhibits multiple signalling pathways involved in cancer cell survival.
In laboratory studies, combining brigatinib with a PARP inhibitor was more effective than either treatment alone. Notably, the effect was seen in cancer cells but not normal cells, suggesting a more targeted approach.
Brigatinib also appeared to act in an unexpected way. Rather than working through the usual DNA repair routes, it shut down two signalling molecules, FAK and EPHA2, that aggressive ovarian cancer cells rely on. FAK and EPHA2 are proteins that relay survival signals inside cells. Blocking both at once weakened the cells’ ability to adapt and resist treatment, making them more vulnerable to PARP inhibitors.
Tumours with higher levels of FAK and EPHA2 responded better to the drug combination. Other data link high levels of these molecules to more aggressive disease, pointing to potential benefit in harder-to-treat cases.
Arun Kanakkanthara, an oncology investigator at Mayo Clinic and a senior author of the study, said: “This work shows that drug resistance does not always emerge slowly over time; cancer cells can activate survival programmes very early after treatment begins.”
John Weroha, a medical oncologist at Mayo Clinic and a senior author of the study, said: “From a clinical perspective, resistance remains one of the biggest challenges in treating ovarian cancer. By combining mechanistic insights from Dr Kanakkanthara’s laboratory with my clinical experience, this preclinical work supports the strategy of targeting resistance early, before it has a chance to take hold. This strategy could improve patient outcomes.”
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