Updated references in papers.bib

_bibliography/papers.bib

@@ -69,42 +69,45 @@ @ARTICLE{Woodward2021-ka
 }
 
 @ARTICLE{Attia2023-bc,
-  title    = "Orthogonal Gelations to Synthesize Core-Shell Hydrogels Loaded
-              with Nanoemulsion-Templated Drug Nanoparticles for Versatile Oral
-              Drug Delivery",
-  author   = "Attia, Lucas and Chen, Liang-Hsun and Doyle, Patrick S",
-  journal  = "Adv. Healthc. Mater.",
-  pages    = "e2301667",
-  abstract = "Hydrophobic active pharmaceutical ingredients are ubiquitous in
-              the drug development pipeline, but their poor bioavailability
-              often prevents their translation into drug products. Industrial
-              processes to formulate hydrophobic APIs are expensive, difficult
-              to optimize, and not flexible enough to incorporate customizable
-              drug release profiles into drug products. Here, a novel,
-              dual-responsive gelation process that exploits orthogonal
-              thermo-responsive and ion-responsive gelations is introduced. This
-              one-step ``dual gelation'' synthesizes core-shell
-              (methylcellulose-alginate) hydrogel particles and encapsulates
-              drug-laden nanoemulsions in the hydrogel matrices. In situ
-              crystallization templates drug nanocrystals inside the polymeric
-              core, while a kinetically stable amorphous solid dispersion is
-              templated in the shell. Drug release is explored as a function of
-              particle geometry, and programmable release is demonstrated for
-              various therapeutic applications including delayed pulsatile
-              release and sequential release of a model fixed-dose combination
-              drug product of ibuprofen and fenofibrate. Independent control
-              over drug loading between the shell and the core is demonstrated.
-              This formulation approach is shown to be a flexible process to
-              develop drug products with biocompatible materials, facile
-              synthesis, and precise drug release performance. This work
-              suggests and applies a novel method to leverage orthogonal gel
-              chemistries to generate functional core-shell hydrogel particles.
-              This article is protected by copyright. All rights reserved.",
-  month    =  jul,
-  year     =  2023,
-  keywords = "drug delivery; hydrogels; nanocrystals; nanoemulsions;
-              stimuli-responsive materials",
-  language = "en"
+  title     = "Orthogonal gelations to synthesize core-shell hydrogels loaded
+               with nanoemulsion-templated drug nanoparticles for versatile oral
+               drug delivery",
+  author    = "Attia, Lucas and Chen, Liang-Hsun and Doyle, Patrick S",
+  journal   = "Adv. Healthc. Mater.",
+  publisher = "Wiley",
+  volume    =  12,
+  number    =  31,
+  pages     = "e2301667",
+  abstract  = "Hydrophobic active pharmaceutical ingredients (APIs) are
+               ubiquitous in the drug development pipeline, but their poor
+               bioavailability often prevents their translation into drug
+               products. Industrial processes to formulate hydrophobic APIs are
+               expensive, difficult to optimize, and not flexible enough to
+               incorporate customizable drug release profiles into drug
+               products. Here, a novel, dual-responsive gelation process that
+               exploits orthogonal thermo-responsive and ion-responsive
+               gelations is introduced. This one-step ``dual gelation''
+               synthesizes core-shell (methylcellulose-alginate) hydrogel
+               particles and encapsulates drug-laden nanoemulsions in the
+               hydrogel matrices. In situ crystallization templates drug
+               nanocrystals inside the polymeric core, while a kinetically
+               stable amorphous solid dispersion is templated in the shell. Drug
+               release is explored as a function of particle geometry, and
+               programmable release is demonstrated for various therapeutic
+               applications including delayed pulsatile release and sequential
+               release of a model fixed-dose combination drug product of
+               ibuprofen and fenofibrate. Independent control over drug loading
+               between the shell and the core is demonstrated. This formulation
+               approach is shown to be a flexible process to develop drug
+               products with biocompatible materials, facile synthesis, and
+               precise drug release performance. This work suggests and applies
+               a novel method to leverage orthogonal gel chemistries to generate
+               functional core-shell hydrogel particles.",
+  month     =  dec,
+  year      =  2023,
+  keywords  = "drug delivery; hydrogels; nanocrystals; nanoemulsions;
+               stimuli-responsive materials",
+  language  = "en"
 }
 
 @ARTICLE{Jarai2020-tn,