2014
DOI: 10.1039/c3cc47666a
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Polyacrylic acid@zeolitic imidazolate framework-8 nanoparticles with ultrahigh drug loading capability for pH-sensitive drug release

Abstract: The polyacrylic acid@zeolitic imidazolate framework-8 (PAA@ZIF-8) nanoparticles (NPs) were first fabricated using a facile and simple route. It is worthwhile noting that the as-fabricated PAA@ZIF-8 NPs possessed ultrahigh doxorubicin (DOX) loading capability (1.9 g DOX g(-1) NPs), which were employed as pH-dependent drug delivery vehicles.

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Cited by 237 publications
(181 citation statements)
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“…As the cavity of the ZIFs frameworks are filled by drug molecules, so they become more rigid and become more thermally 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 13 Therefore, it is clear from IR, UV, TGA and PXRD data that drug is incorporated inside the ZIFs framework. It is noteworthy that although ZIF-8 has been used as a DDS for camptothecin and other drug molecules as reported earlier, [43][44][45] there are no such reports where drug ...…”
Section: Figure 1: Sem Images Of (A) Zif-7 (B) Zif-8 Nanospheresmentioning
confidence: 92%
“…As the cavity of the ZIFs frameworks are filled by drug molecules, so they become more rigid and become more thermally 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 13 Therefore, it is clear from IR, UV, TGA and PXRD data that drug is incorporated inside the ZIFs framework. It is noteworthy that although ZIF-8 has been used as a DDS for camptothecin and other drug molecules as reported earlier, [43][44][45] there are no such reports where drug ...…”
Section: Figure 1: Sem Images Of (A) Zif-7 (B) Zif-8 Nanospheresmentioning
confidence: 92%
“…HMNPs and the applications in simultaneous fluorescence, MR imaging and drug delivery are presented in Scheme 1. Briefly, the PAAS NPs were firstly synthesized by using a facile and mild route in a deionized water (DI water)-isopropyl alcohol (IPA) (volume ratio = 1:4) system at room temperature [42]. After successively adding Gd(NO 3 ) 3 After calcination at 600 °C for 5h, the PAAS NPs templates were removed, Gd(OH) 3 and Eu(OH) 3 were transferred to Gd 2 O 3 and Eu 2 O 3 after thermal decomposition, resulting in the formation of well-dispersed Eu 3+ -doped Gd 2 O 3 HMNPs.…”
Section: Resultsmentioning
confidence: 99%
“…2A (a), (b) and (c) show the FT-IR spectra of PAAS NPs, PAA@Gd(OH) 3 /Eu(OH) 3 precursors and Eu 3+ -doped Gd 2 O 3 HMNPs, respectively. The obvious peaks appeared at 1560 and 1410 cm -1 in PAAS NPs and PAA@Gd(OH) 3 /Eu(OH) 3 precursors are assigned to the shift of the C=O bands caused by coordination of -COO -groups and metal cations, qualitativelyindicating the presence of PAA[42]. For Eu 3+ -doped Gd 2 O 3 HMNPs, the band around 1500 cm -1 attributed to -COO -stretching vibration almost disappeared, confirming that the PAAS templates have been removed successfully from the obtained HMNPs.In addition, the peak appeared at 550 cm -1 which results from the Gd-O vibration of cubic Gd 2 O 3 is obviously found from the curve of Eu 3+ -doped Gd 2 O 3 HMNPs[43].The aforementioned results strongly suggest that the PAA@Gd(OH)3 /Eu(OH) 3 precursors have successfully converted to Eu 3+ -doped Gd 2 O 3 HMNPs during the (curve b), which further affirm the transformation from amorphous PAA@Gd(OH) 3 /Eu(OH) 3 precursors to highly crystalline Eu 3+ -doped Gd 2 O 3 HMNPs.…”
mentioning
confidence: 94%
“…2C. The first event is the loss of PAA at a temperature range of 400-440°C, 12 and the second event takes place at a temperature range of 600-750°C, which is consistent with the typical weight loss of CaCO 3 . 13 The XRD pattern of the obtained PAA/CaCO 3 NPs shows no obvious diffraction peak, as shown in Fig.…”
mentioning
confidence: 88%